SAFE AID DEVICE IMPOTENCE DEVICE— 510(k) K896357

Name: FDA 510(k) clearance K896357
Creator: U.S. Food and Drug Administration
Published: 1990-04-25

Substantially Equivalent

Dr. John P. March

FDA 510(k) clearance K896357 for SAFE AID DEVICE IMPOTENCE DEVICE, Substantially Equivalent on 1990-04-25. Applicant: Dr. John P. March. Device class: 2.

Clearance details

Applicant: Dr. John P. March
Product code: Code LKY
Device class: Class 2
Regulation: 21 CFR 876.5020
Advisory panel: Gastroenterology, Urology
Date received: 1989-11-06
Decision date: 1990-04-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sacramento, CA, US

Download summary PDF View on FDA.gov ↗

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K030913 — NANMA VACUUM PUMP2003-06-03
K013113 — MODIFICATION TO NANMA VACUUM PUMP2002-12-20

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