PULSELIFE STIMULATOR— 510(k) K840983

Name: FDA 510(k) clearance K840983
Creator: U.S. Food and Drug Administration
Published: 1984-03-27

Substantially Equivalent

Pulse Life, Inc.

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

Clearance details

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

Download summary PDF View on FDA.gov ↗

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