KEITHLEY LYMPHOCYTE DEPLETION CART— 510(k) K801899

Name: FDA 510(k) clearance K801899
Creator: U.S. Food and Drug Administration
Published: 1980-09-26

Substantially Equivalent

Keithley Development Co.

FDA 510(k) clearance K801899 for KEITHLEY LYMPHOCYTE DEPLETION CART, Substantially Equivalent on 1980-09-26. Applicant: Keithley Development Co.. Device class: 2.

Clearance details

Applicant: Keithley Development Co.
Product code: Code KDK
Device class: Class 2
Regulation: 21 CFR 876.5880
Advisory panel: Gastroenterology, Urology
Date received: 1980-08-08
Decision date: 1980-09-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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