Cleared Traditional

K862145 - JEDMED MINI-MOS VIDEO CAMERA (FDA 510(k) Clearance)

Class I General & Plastic Surgery device.

K862145 · Jedmed Instrument Co. · General & Plastic Surgery device
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Jun 1986
Decision
9d
Days
Class 1
Risk

K862145 is an FDA 510(k) clearance for the JEDMED MINI-MOS VIDEO CAMERA. Classified as Camera, Television, Microsurgical, Without Audio (product code FWD), Class I - General Controls.

Submitted by Jedmed Instrument Co. (St. Louis, US). The FDA issued a Cleared decision on June 13, 1986 after a review of 9 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 Jedmed Instrument Co. devices

Submission Details

510(k) Number K862145 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 04, 1986
Decision Date June 13, 1986
Days to Decision 9 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
105d faster than avg
Panel avg: 114d · This submission: 9d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code FWD Camera, Television, Microsurgical, Without Audio
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.