BIOSENSOR BIDOP VASCULAR TEST SYSTEM— 510(k) K943338

Substantially Equivalent

Biosensor Corp.

FDA 510(k) clearance K943338 for BIOSENSOR BIDOP VASCULAR TEST SYSTEM, Substantially Equivalent on 1996-04-12. Applicant: Biosensor Corp.. Device class: 2.

Clearance details

Applicant
Biosensor Corp.
Product code
Code JAF
Device class
Class 2
Regulation
21 CFR 892.1540
Advisory panel
Radiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Minneapolis, MN, US
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