DEXIDE DIS. PREP SPONGE W/IDEX PATIENT P— 510(k) K792273

Name: FDA 510(k) clearance K792273
Creator: U.S. Food and Drug Administration
Published: 1979-12-10

Substantially Equivalent

Dexide, Inc.

FDA 510(k) clearance K792273 for DEXIDE DIS. PREP SPONGE W/IDEX PATIENT P, Substantially Equivalent on 1979-12-10. Applicant: Dexide, Inc.. Device class: 1.

Clearance details

Applicant: Dexide, Inc.
Product code: Code GEC
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1979-11-13
Decision date: 1979-12-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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