BANDAGE, MUSLIN, COMPRESSED, CAMOUFLAGED, 37X37X52— 510(k) K891998

Name: FDA 510(k) clearance K891998
Creator: U.S. Food and Drug Administration
Published: 1989-06-05

Substantially Equivalent

Elwyn Industries

FDA 510(k) clearance K891998 for BANDAGE, MUSLIN, COMPRESSED, CAMOUFLAGED, 37X37X52, Substantially Equivalent on 1989-06-05. Applicant: Elwyn Industries. Device class: 1.

Clearance details

Applicant: Elwyn Industries
Product code: Code NAD
Device class: Class 1
Regulation: 21 CFR 878.4020
Advisory panel: General, Plastic Surgery
Date received: 1989-03-28
Decision date: 1989-06-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Philadelphia, PA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code NAD

product code NAD

Injury: 431
Malfunction: 11,935
Other: 1
Total: 12,367

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.