SAFE-TEC CAPILLARY BLOOD COLLECTION TUBE— 510(k) K884623

Name: FDA 510(k) clearance K884623
Creator: U.S. Food and Drug Administration
Published: 1988-12-01

Substantially Equivalent

Safe-Tec Clinical Products, Inc.

FDA 510(k) clearance K884623 for SAFE-TEC CAPILLARY BLOOD COLLECTION TUBE, Substantially Equivalent on 1988-12-01. Applicant: Safe-Tec Clinical Products, Inc.. Device class: 1.

Clearance details

Applicant: Safe-Tec Clinical Products, Inc.
Product code: Code GIO
Device class: Class 1
Regulation: 21 CFR 864.6150
Advisory panel: Hematology
Date received: 1988-11-04
Decision date: 1988-12-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ivyland, PA, US

Download summary PDF View on FDA.gov ↗

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