Cleared Traditional

AUTOCLAVEABLE MEDICAM 900 DIGICON CAMERA (K942358) - FDA 510(k) Clearance

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

K942358 · M.P. Video, Inc. · General & Plastic Surgery device
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Aug 1994
Decision
83d
Days
Class 2
Risk

K942358 is an FDA 510(k) clearance for the AUTOCLAVEABLE MEDICAM 900 DIGICON CAMERA. 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 August 8, 1994 after a review of 83 days - a notably fast clearance cycle.

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: 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 M.P. Video, Inc. devices

Submission Details

510(k) Number K942358 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 17, 1994
Decision Date August 08, 1994
Days to Decision 83 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
32d faster than avg
Panel avg: 115d · This submission: 83d
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 K942358.
CCD ENDOCAM OFFICE 5510
K942817 · Richard Wolf Medical Instruments Corp. · Aug 1994
KARL STORZ WOUND CLOSURE INSTRUMENTS
K942612 · KARL STORZ Endoscopy-America, Inc. · Aug 1994
OPSIS THORACOSCOPY VIDEO SYSTEM THORACICCAM AND THORACICCAM 360
K941950 · Baxter Healthcare Corp · Aug 1994
OLYMPUS SUPERVIEW LAPAROSCOPE FOR GENERAL SURGERY
K942839 · Olympus America, Inc. · Jul 1994
AESCULAP FLEXIBLE TROCAR INSTRUMENT SET
K935243 · Aesculap, Inc. · Jul 1994
ANGLED DISSECTORS MODELS 8383.581/582/571
K940948 · Richard Wolf Medical Instruments Corp. · Jul 1994