SPONGE, LAPAROTOMY GAUZE— 510(k) K760113

Name: FDA 510(k) clearance K760113
Creator: U.S. Food and Drug Administration
Published: 1976-07-15

Substantially Equivalent

Parke-Davis Co.

FDA 510(k) clearance K760113 for SPONGE, LAPAROTOMY GAUZE, Substantially Equivalent on 1976-07-15. Applicant: Parke-Davis Co.. Device class: Unclassified.

Clearance details

Applicant: Parke-Davis Co.
Product code: Code EFQ
Device class: Unclassified
Advisory panel: Unknown
Date received: 1976-06-24
Decision date: 1976-07-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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