PULSAR NEUROSTIMULATOR— 510(k) K852061

Substantially Equivalent

Andromeda Research, Inc.

FDA 510(k) clearance K852061 for PULSAR NEUROSTIMULATOR, Substantially Equivalent on 1986-07-18. Applicant: Andromeda Research, Inc..

Clearance details

Applicant: Andromeda Research, Inc.
Product code: Code GZJ
Advisory panel: Neurology
Date received: 1985-05-09
Decision date: 1986-07-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Oyster Bay, NY, US

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