CONVERTORS STERILE DISP. LAP SPONGE II— 510(k) K813296

Name: FDA 510(k) clearance K813296
Creator: U.S. Food and Drug Administration
Published: 1981-12-29

Substantially Equivalent

American Convertors Div., American Pharmaseal

FDA 510(k) clearance K813296 for CONVERTORS STERILE DISP. LAP SPONGE II, Substantially Equivalent on 1981-12-29. Applicant: American Convertors Div., American Pharmaseal. Device class: Unclassified.

Clearance details

Applicant: American Convertors Div., American Pharmaseal
Product code: Code EFQ
Device class: Unclassified
Advisory panel: Unknown
Date received: 1981-11-23
Decision date: 1981-12-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, 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.