Cleared Traditional

K782092 - ARMBOARD CVER

K782092 is an FDA 510(k) clearance for ARMBOARD CVER, manufactured by Anago, Inc.. The device is a Class 1 General & Plastic Surgery device with product code FSE cleared through the Traditional 510(k) pathway after a 27-day FDA review.

K782092 · Anago, Inc. · General & Plastic Surgery device
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Jan 1979
Decision
27d
Days
Class 1
Risk

K782092 is an FDA 510(k) clearance for the ARMBOARD CVER, DISPOSABLE. Classified as Table, Operating-room, Manual (product code FSE), Class I - General Controls.

Submitted by Anago, Inc. (Mchenry, US). The FDA issued a Cleared decision on January 10, 1979 after a review of 27 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4950 - 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 Anago, Inc. devices

FDA 510(k) Submission Details - K782092

510(k) Number K782092 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 14, 1978
Decision Date January 10, 1979
Days to Decision 27 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
88d faster than avg
Panel avg: 115d · This submission: 27d
Pathway characteristics
Predicate-based equivalence.

FSE Device Classification - Class 1, General Controls

Product Code FSE Table, Operating-room, Manual
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4950
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 - FSE Table, Operating-room, Manual

Devices cleared under the same product code (FSE) and FDA review panel - the closest regulatory comparables to K782092.
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