BEMIS ONE QUART PHLEBOTOMY CONTAINER (PART NUMBER 100)— 510(k) K960525

Name: FDA 510(k) clearance K960525
Creator: U.S. Food and Drug Administration
Published: 1996-03-28

Substantially Equivalent

Bemis Mfg. Co.

FDA 510(k) clearance K960525 for BEMIS ONE QUART PHLEBOTOMY CONTAINER (PART NUMBER 100), Substantially Equivalent on 1996-03-28. Applicant: Bemis Mfg. Co.. Device class: 2.

Clearance details

Applicant: Bemis Mfg. Co.
Product code: Code MMK
Device class: Class 2
Regulation: 21 CFR 880.5570
Advisory panel: General Hospital
Date received: 1996-02-05
Decision date: 1996-03-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sheboygan Falls, WI, US

Download summary PDF View on FDA.gov ↗

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