POST OPERATIVE SPONGE— 510(k) K912693

Substantially Equivalent

Ulti-Med Intl., Inc.

FDA 510(k) clearance K912693 for POST OPERATIVE SPONGE, Substantially Equivalent on 1991-10-04. Applicant: Ulti-Med Intl., Inc.. Device class: 1.

Clearance details

Applicant: Ulti-Med Intl., Inc.
Product code: Code NAB
Device class: Class 1
Regulation: 21 CFR 878.4014
Advisory panel: General, Plastic Surgery
Date received: 1991-06-18
Decision date: 1991-10-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Glendale Hts., IL, US

Download summary PDF View on FDA.gov ↗

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