THROMBO-SCREEN PLATELET ADHESION— 510(k) K771678

Name: FDA 510(k) clearance K771678
Creator: U.S. Food and Drug Administration
Published: 1977-11-22

Substantially Equivalent

Bay Area Hema. Onco. Clinic. & Res. L

FDA 510(k) clearance K771678 for THROMBO-SCREEN PLATELET ADHESION, Substantially Equivalent on 1977-11-22. Applicant: Bay Area Hema. Onco. Clinic. & Res. L. Device class: 2.

Clearance details

Applicant: Bay Area Hema. Onco. Clinic. & Res. L
Product code: Code JBZ
Device class: Class 2
Regulation: 21 CFR 864.6650
Advisory panel: Hematology
Date received: 1977-09-02
Decision date: 1977-11-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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K771523 — LATELET RETENTION COLUMN1977-11-22

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K770395 — THROMBO-CETIN (RISTOCETIN)1977-03-21

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