PLEXUS PULSER I, PLEXUS PULSER II— 510(k) K924891

Substantially Equivalent

Dobre, Inc.

FDA 510(k) clearance K924891 for PLEXUS PULSER I, PLEXUS PULSER II, Substantially Equivalent on 1993-06-07. Applicant: Dobre, Inc..

Clearance details

Applicant: Dobre, Inc.
Product code: Code JOW
Advisory panel: Cardiovascular
Date received: 1992-09-28
Decision date: 1993-06-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kettering, OH, US

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