PULSELIFE STIMULATOR— 510(k) K840983

Substantially Equivalent

Pulse Life, Inc.

FDA 510(k) clearance K840983 for PULSELIFE STIMULATOR, Substantially Equivalent on 1984-03-27. Applicant: Pulse Life, Inc..

Clearance details

Applicant: Pulse Life, Inc.
Product code: Code BWK
Advisory panel: Unknown
Date received: 1984-03-06
Decision date: 1984-03-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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