IMMU-TEK AUTOMATIC CENTRIFUGE— 510(k) K790767

Name: FDA 510(k) clearance K790767
Creator: U.S. Food and Drug Administration
Published: 1979-05-23

Substantially Equivalent

Dade, Baxter Travenol Diagnostics, Inc.

FDA 510(k) clearance K790767 for IMMU-TEK AUTOMATIC CENTRIFUGE, Substantially Equivalent on 1979-05-23. Applicant: Dade, Baxter Travenol Diagnostics, Inc.. Device class: 2.

Clearance details

Applicant: Dade, Baxter Travenol Diagnostics, Inc.
Product code: Code KSN
Device class: Class 2
Regulation: 21 CFR 864.9285
Advisory panel: Hematology
Date received: 1979-04-19
Decision date: 1979-05-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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