Cleared Traditional

K936086 - STERILE VIDEO CAMERA COVER AND DRAPE

K936086 is the FDA 510(k) clearance for STERILE VIDEO CAMERA COVER AND DRAPE by Micromedical Devices, Inc.. It is a Class 2 Radiology device (product code KXK) cleared through the Traditional 510(k) pathway after a 86-day FDA review.

K936086 · Micromedical Devices, Inc. · Radiology device
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Mar 1994
Decision
86d
Days
Class 2
Risk

K936086 is an FDA 510(k) clearance for the STERILE VIDEO CAMERA COVER AND DRAPE. Classified as Source, Brachytherapy, Radionuclide (product code KXK), Class II - Special Controls.

Submitted by Micromedical Devices, Inc. (Castle Pines Village, US). The FDA issued a Cleared decision on March 17, 1994 after a review of 86 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.5730 - the FDA radiology and imaging software oversight 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 Micromedical Devices, Inc. devices

Submission Details

510(k) Number K936086 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 21, 1993
Decision Date March 17, 1994
Days to Decision 86 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
21d faster than avg
Panel avg: 107d · This submission: 86d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code KXK Source, Brachytherapy, Radionuclide
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.5730
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 Radiology devices follow this clearance model.

Regulatory Peers - KXK Source, Brachytherapy, Radionuclide

All 30
Devices cleared under the same product code (KXK) and FDA review panel - the closest regulatory comparables to K936086.
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