Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name Device, External Penile Rigidity
510(k) Number K844445
Device Name REVIVE SYSTEM
Applicant
Revive Systems Corp.
2101 L St. NW
Washington,  DC  20037
Applicant Contact RODNEY R MUNSEY
Correspondent
Revive Systems Corp.
2101 L St. NW
Washington,  DC  20037
Correspondent Contact RODNEY R MUNSEY
Regulation Number876.5020
Classification Product Code
LKY  
Date Received11/16/1984
Decision Date 09/17/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-