CIRCULON SYSTEM STEP 1— 510(k) K951022

Name: FDA 510(k) clearance K951022
Creator: U.S. Food and Drug Administration
Published: 1995-06-12

Unknown

Convatec, A Division of E.R. Squibb & Sons

FDA 510(k) clearance K951022 for CIRCULON SYSTEM STEP 1, Unknown on 1995-06-12. Applicant: Convatec, A Division of E.R. Squibb & Sons. Device class: 2.

Clearance details

Applicant: Convatec, A Division of E.R. Squibb & Sons
Product code: Code MCY
Device class: Class 2
Regulation: 21 CFR 880.5075
Advisory panel: General Hospital
Date received: 1995-03-07
Decision date: 1995-06-12
Decision: Unknown
Clearance type: Traditional
Location: Princeton, NJ, US

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