MEDICAL PRODUCTS FOAM DOUBLE SCRUB #450— 510(k) K831226

Name: FDA 510(k) clearance K831226
Creator: U.S. Food and Drug Administration
Published: 1983-05-16

Substantially Equivalent

Ballard Medical Products

FDA 510(k) clearance K831226 for MEDICAL PRODUCTS FOAM DOUBLE SCRUB #450, Substantially Equivalent on 1983-05-16. Applicant: Ballard Medical Products. Device class: 1.

Clearance details

Applicant: Ballard Medical Products
Product code: Code GEC
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1983-04-15
Decision date: 1983-05-16
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.