ABIOMED PERIOTEMP(TM) PROBE— 510(k) K885075

Substantially Equivalent

Abiomed, Inc.

FDA 510(k) clearance K885075 for ABIOMED PERIOTEMP(TM) PROBE, Substantially Equivalent on 1989-02-13. Applicant: Abiomed, Inc..

Clearance details

Applicant: Abiomed, Inc.
Product code: Code EIL
Advisory panel: Dental
Date received: 1988-12-08
Decision date: 1989-02-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Danvers, MA, US

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