INTRAVENOUS START KIT— 510(k) K843813

Substantially Equivalent

Pro-Lab, Inc.

FDA 510(k) clearance K843813 for INTRAVENOUS START KIT, Substantially Equivalent on 1984-12-05. Applicant: Pro-Lab, Inc..

Clearance details

Applicant: Pro-Lab, Inc.
Advisory panel: Unknown
Date received: 1984-09-28
Decision date: 1984-12-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Round Rock, TX, US

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