SEAGER ELECTROEJACULATOR— 510(k) K962379

Name: FDA 510(k) clearance K962379
Creator: U.S. Food and Drug Administration
Published: 1997-09-18

Substantially Equivalent

National Rehab Hospital

FDA 510(k) clearance K962379 for SEAGER ELECTROEJACULATOR, Substantially Equivalent on 1997-09-18. Applicant: National Rehab Hospital. Device class: Unclassified.

Clearance details

Applicant: National Rehab Hospital
Product code: Code LNL
Device class: Unclassified
Advisory panel: Unknown
Date received: 1996-06-20
Decision date: 1997-09-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

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