Cleared Traditional

K953286 - FCP-9P

K953286 is the FDA 510(k) clearance for FCP-9P by Pentax Precision Instrument Corp.. It is a Class 2 Gastroenterology & Urology device (product code FBN) cleared through the Traditional 510(k) pathway after a 113-day FDA review.

K953286 · Pentax Precision Instrument Corp. · Gastroenterology & Urology device
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Optimized for regulatory review, auditing and printing
Nov 1995
Decision
113d
Days
Class 2
Risk

K953286 is an FDA 510(k) clearance for the FCP-9P, FIBER CHOLEDOCHOSCOPE. Classified as Choledochoscope And Accessories, Flexible/rigid (product code FBN), Class II - Special Controls.

Submitted by Pentax Precision Instrument Corp. (Miramar, US). The FDA issued a Cleared decision on November 3, 1995 after a review of 113 days - within the typical 510(k) review window.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.1500 - the FDA gastroenterology and urology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Gastroenterology & Urology review framework, consistent with the majority of Class II 510(k) submissions.

View all Pentax Precision Instrument Corp. devices

Submission Details

510(k) Number K953286 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 13, 1995
Decision Date November 03, 1995
Days to Decision 113 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
17d faster than avg
Panel avg: 130d · This submission: 113d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code FBN Choledochoscope And Accessories, Flexible/rigid
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.1500
Definition To Examine And Perform Procedures Within The Bile Ducts. For Reusable, Flexible Endoscopes In This Product Code, Validated Reprocessing Instructions And Reprocessing Validation Data Must Be Included In A 510(k) Submission (82 Fr 26807, Available At Https://www.gpo.gov/fdsys/pkg/fr-2017-06-09/pdf/2017-12007.pdf).
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Gastroenterology & Urology devices follow this clearance model.

Regulatory Peers - FBN Choledochoscope And Accessories, Flexible/rigid

All 35
Devices cleared under the same product code (FBN) and FDA review panel - the closest regulatory comparables to K953286.
KSEA 15.5 FR. FLEXIBLE CHOLEDOCHO-FIBERSCOPE
K971977 · KARL STORZ Endoscopy-America, Inc. · Aug 1997
FLEXIBLE MINI-FIBERSCOPES
K962172 · Richard Wolf Medical Instruments Corp. · Dec 1996
XCHF-33 CHOLEDOCHOFIBERSCOPE
K944473 · Olympus America, Inc. · Nov 1995
FCN-15X, FIBER CHOLEDOCHONEPHROSCOPE
K951191 · Pentax Precision Instrument Corp. · May 1995
KARL STORZ FLEXIBLE CHOLEDOCHOSCOPE
K942112 · Karl Storz Endoscopy · Feb 1995
CHOLEDOCHOSCOPE/ENDOSCOPE MODIFICATION
K933906 · Fujinon, Inc. · Jul 1994