Cleared Traditional

MEDICAL DYNAMICS CCD SOLID STATE VIDEO CAMERA 5930 (K855020) - FDA 510(k) Clearance

Class I General & Plastic Surgery device.

K855020 · Medline Industries, Inc. · General & Plastic Surgery device
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Jan 1986
Decision
39d
Days
Class 1
Risk

K855020 is an FDA 510(k) clearance for the MEDICAL DYNAMICS CCD SOLID STATE VIDEO CAMERA 5930. Classified as Camera, Television, Surgical, Without Audio (product code FWB), Class I - General Controls.

Submitted by Medline Industries, Inc. (Englewood, US). The FDA issued a Cleared decision on January 24, 1986 after a review of 39 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 Medline Industries, Inc. devices

Submission Details

510(k) Number K855020 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 16, 1985
Decision Date January 24, 1986
Days to Decision 39 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
76d faster than avg
Panel avg: 115d · This submission: 39d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code FWB Camera, Television, Surgical, 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.