Cleared Traditional

K832342 - ENDOSCOPIC CAMERA TV W/AUDIO (FDA 510(k) Clearance)

Class I General & Plastic Surgery device.

K832342 · Kamiya Tsusan Kaisha, Ltd. · General & Plastic Surgery device
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Sep 1983
Decision
62d
Days
Class 1
Risk

K832342 is an FDA 510(k) clearance for the ENDOSCOPIC CAMERA TV W/AUDIO. Classified as Camera, Surgical And Accessories (product code KQM), Class I - General Controls.

Submitted by Kamiya Tsusan Kaisha, Ltd. (Tokyo 100-91 Japan, US). The FDA issued a Cleared decision on September 12, 1983 after a review of 62 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4160 - 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 Kamiya Tsusan Kaisha, Ltd. devices

Submission Details

510(k) Number K832342 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 12, 1983
Decision Date September 12, 1983
Days to Decision 62 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
52d faster than avg
Panel avg: 114d · This submission: 62d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code KQM Camera, Surgical And Accessories
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4160
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.