Cleared Traditional

K851798 - 53-160 TO 53-167 VARIOUS BIOPSY FORCEPS YEOMAN

K851798 is an FDA 510(k) clearance for 53-160 TO 53-167 VARIOUS BIOPSY FORCEPS..., manufactured by Artiberia. The device is a Class 2 Gastroenterology & Urology device with product code KNW cleared through the Traditional 510(k) pathway after a 28-day FDA review.

K851798 · Artiberia · Gastroenterology & Urology device
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May 1985
Decision
28d
Days
Class 2
Risk

K851798 is an FDA 510(k) clearance for the 53-160 TO 53-167 VARIOUS BIOPSY FORCEPS YEOMAN. Classified as Instrument, Biopsy (product code KNW), Class II - Special Controls.

Submitted by Artiberia (San Antonio, US). The FDA issued a Cleared decision on May 23, 1985 after a review of 28 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.1075 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Artiberia devices

FDA 510(k) Submission Details - K851798

510(k) Number K851798 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 25, 1985
Decision Date May 23, 1985
Days to Decision 28 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
103d faster than avg
Panel avg: 131d · This submission: 28d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KNW Device Classification - Class 2, Special Controls

Product Code KNW Instrument, Biopsy
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.1075
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 - KNW Instrument, Biopsy

All 323
Devices cleared under the same product code (KNW) and FDA review panel - the closest regulatory comparables to K851798.
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