VED VALU- VACUUM ERECTION DEVICE— 510(k) K980948

Name: FDA 510(k) clearance K980948
Creator: U.S. Food and Drug Administration
Published: 1998-06-25

Substantially Equivalent

Mission Pharmacal Comp

FDA 510(k) clearance K980948 for VED VALU- VACUUM ERECTION DEVICE, Substantially Equivalent on 1998-06-25. Applicant: Mission Pharmacal Comp. Device class: 2.

Clearance details

Applicant: Mission Pharmacal Comp
Product code: Code LKY
Device class: Class 2
Regulation: 21 CFR 876.5020
Advisory panel: Gastroenterology, Urology
Date received: 1998-03-13
Decision date: 1998-06-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

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Data sourced from openFDA. This site is unofficial and independent of the FDA.