VACUUM ERECTION DEVICE (VED)— 510(k) K901223

Name: FDA 510(k) clearance K901223
Creator: U.S. Food and Drug Administration
Published: 1990-05-04

Substantially Equivalent

Mission Pharmacal Co.

FDA 510(k) clearance K901223 for VACUUM ERECTION DEVICE (VED), Substantially Equivalent on 1990-05-04. Applicant: Mission Pharmacal Co.. Device class: 2.

Clearance details

Applicant: Mission Pharmacal Co.
Product code: Code LKY
Device class: Class 2
Regulation: 21 CFR 876.5020
Advisory panel: Gastroenterology, Urology
Date received: 1990-03-14
Decision date: 1990-05-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Antonio, TX, US

Download summary PDF View on FDA.gov ↗

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