REGULATOR VENOSET W/0.22 MICRON IVEX— 510(k) K810029

Unknown

Abbott Laboratories

FDA 510(k) clearance K810029 for REGULATOR VENOSET W/0.22 MICRON IVEX, Unknown on 1981-01-06. Applicant: Abbott Laboratories.

Clearance details

Applicant: Abbott Laboratories
Advisory panel: Unknown
Date received: 1981-01-06
Decision date: 1981-01-06
Decision: Unknown
Clearance type: Traditional
Location: Abbott Park, IL, US

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