• 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 condom
510(k) Number K993396
Device Name REMED MALE EXTRA STRENGTH CONDOM PREVENTOR, LUCKY BOY, SUMMIT
Applicant
REMED PHARMA
PO BOX 4341
crofton,  MD  21114
Applicant Contact e.j. smith
Correspondent
REMED PHARMA
PO BOX 4341
crofton,  MD  21114
Correspondent Contact e.j. smith
Regulation Number884.5300
Classification Product Code
HIS  
Date Received10/08/1999
Decision Date 02/15/2000
Decision substantially equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
statement statement
Type Abbreviated
Reviewed by Third Party No
Combination Product No
-
-