BROADLINE OR TOWELS— 510(k) K991667

Name: FDA 510(k) clearance K991667
Creator: U.S. Food and Drug Administration
Published: 1999-09-27

Substantially Equivalent

Broadline Medical Industries

FDA 510(k) clearance K991667 for BROADLINE OR TOWELS, Substantially Equivalent on 1999-09-27. Applicant: Broadline Medical Industries. Device class: 2.

Clearance details

Applicant: Broadline Medical Industries
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1999-05-14
Decision date: 1999-09-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Inverness, IL, US

Download summary PDF View on FDA.gov ↗

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