Cleared Traditional

COMBINATION CAMERA/LIGHT SOURCE (K951386) - FDA 510(k) Clearance

Class II General & Plastic Surgery device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K951386 · M.P. Video, Inc. · General & Plastic Surgery device
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Jun 1995
Decision
95d
Days
Class 2
Risk

K951386 is an FDA 510(k) clearance for the COMBINATION CAMERA/LIGHT SOURCE. Classified as Laparoscope, General & Plastic Surgery (product code GCJ), Class II - Special Controls.

Submitted by M.P. Video, Inc. (Medway, US). The FDA issued a Cleared decision on June 30, 1995 after a review of 95 days - within the typical 510(k) review window.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 876.1500 - the FDA general and plastic surgery 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 General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

View all M.P. Video, Inc. devices

Submission Details

510(k) Number K951386 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 27, 1995
Decision Date June 30, 1995
Days to Decision 95 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
20d faster than avg
Panel avg: 115d · This submission: 95d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code GCJ Laparoscope, General & Plastic Surgery
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.1500
Definition Validated Reprocessing Instructions And Reprocessing Validation Data For This Device Type Must Be Included In A 510(k) Submission If The Device Is Reusable And Has Specific Design Features (please Refer To Table 2 Of 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 General & Plastic Surgery devices follow this clearance model.

Regulatory Peers - GCJ Laparoscope, General & Plastic Surgery

All 399
Devices cleared under the same product code (GCJ) and FDA review panel - the closest regulatory comparables to K951386.
KARL STORZ ENDOSCOPY POWDER BLOWER
K952443 · KARL STORZ Endoscopy-America, Inc. · Aug 1995
QUESTUS DISPOSABLE ENDOSCOPIC KNIFE
K952926 · Wrightmedicaltechnologyinc · Jul 1995
ETHICON ARTHROSCOPIC KNOT PUSHER
K952814 · Ethicon, Inc. · Jul 1995
INSULATED ELECTROSURGICAL INSTRUMENTS
K951986 · KARL STORZ Endoscopy-America, Inc. · Jun 1995
KARL STORZ KOH NEEDLE HOLDERS, FORCEPS FOR SUTURING, SUTURE SCISSORS, TISSUE PROBES, INJECTION NEEDLE, IRRIGATION INSTRT
K951625 · KARL STORZ Endoscopy-America, Inc. · May 1995
ENDO IRRIGATOR 2211, INCLUDING TUBING
K951715 · Richard Wolf Medical Instruments Corp. · May 1995