Cleared Traditional

K872661 - RGB CAMERA SYSTEM

K872661 is an FDA 510(k) clearance for RGB CAMERA SYSTEM, manufactured by Aspen Laboratories, Inc.. The device is a Class 1 General & Plastic Surgery device with product code FWF cleared through the Traditional 510(k) pathway after a 14-day FDA review.

K872661 · Aspen Laboratories, Inc. · General & Plastic Surgery device
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Jul 1987
Decision
14d
Days
Class 1
Risk

K872661 is an FDA 510(k) clearance for the RGB CAMERA SYSTEM. Classified as Camera, Television, Endoscopic, Without Audio (product code FWF), Class I - General Controls.

Submitted by Aspen Laboratories, Inc. (Englewood, US). The FDA issued a Cleared decision on July 21, 1987 after a review of 14 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 Aspen Laboratories, Inc. devices

FDA 510(k) Submission Details - K872661

510(k) Number K872661 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 07, 1987
Decision Date July 21, 1987
Days to Decision 14 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
101d faster than avg
Panel avg: 115d · This submission: 14d
Pathway characteristics
Predicate-based equivalence.

FWF Device Classification - Class 1, General Controls

Product Code FWF Camera, Television, Endoscopic, 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.

Regulatory Peers - FWF Camera, Television, Endoscopic, Without Audio

All 7
Devices cleared under the same product code (FWF) and FDA review panel - the closest regulatory comparables to K872661.
VIDEO CAMERA W/ ELECTRONIC SHUTTER MODEL VCE-10
K930053 · Medical Devices, Inc. · May 1993
INTEGRATED VISUALIZATION SYSTEM
K925108 · Neuro Navigational Corp. · Jan 1993
THE KARL STORZ MINI 9000 SOLID STATE CCD VIDEO CAM
K881014 · KARL STORZ Endoscopy-America, Inc. · Apr 1988
VIDEO CAMERA SYSTEM
K863598 · American Edwards Laboratories · Oct 1986
ARTHROSCAN VIDEO SYSTEM
K834069 · Concept, Inc. · Jan 1984