CAMPYPAK— 510(k) K811957

Name: FDA 510(k) clearance K811957
Creator: U.S. Food and Drug Administration
Published: 1981-07-23

Substantially Equivalent

Bd Becton Dickinson Vacutainer Systems Preanalytic

FDA 510(k) clearance K811957 for CAMPYPAK, Substantially Equivalent on 1981-07-23. Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic. Device class: 1.

Clearance details

Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic
Product code: Code KZJ
Device class: Class 1
Regulation: 21 CFR 866.2580
Advisory panel: Microbiology
Date received: 1981-07-09
Decision date: 1981-07-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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