Medical Device Manufacturer · US , Crofton , MD

Remed Pharma - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 2000
9
Total
9
Cleared
0
Denied

Remed Pharma has 9 FDA 510(k) cleared medical devices. Based in Crofton, US.

Historical record: 9 cleared submissions from 2000 to 2000. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by Remed Pharma Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Remed Pharma

9 devices
1-9 of 9
Cleared Aug 18, 2000
REMED MALE TUTTI FRUTTI CONDOM (BANANA), PREVENTOR, LUCKY BOY, SUMMIT
K993389 · HIS
Obstetrics & Gynecology · 315d
Cleared Aug 18, 2000
REMED MALE TUTTI FRUTTI CONDOM (STRAWBERRY) PREVENTOR, LUCKY BOY, SUMMIT
K993403 · HIS
Obstetrics & Gynecology · 315d
Cleared Aug 18, 2000
REMED MALE TUTTI FRUTTI CONDOM (COCONUT) PREVENTOR, LUCKY BOY, SUMMIT
K993409 · HIS
Obstetrics & Gynecology · 315d
Cleared Feb 15, 2000
REMED MALE LATEX CONDOM (DOUBLE WHOOPER) PREVENTOR, LUCKY BOY AND SUMMIT
K993395 · HIS
Obstetrics & Gynecology · 130d
Cleared Feb 15, 2000
REMED MALE EXTRA STRENGTH CONDOM PREVENTOR, LUCKY BOY, SUMMIT
K993396 · HIS
Obstetrics & Gynecology · 130d
Cleared Feb 15, 2000
REMED MALE LATEX CONDOM (CLASSIC) PREVENTOR, LUCKY BOY, AND SUMMIT
K993404 · HIS
Obstetrics & Gynecology · 130d
Cleared Feb 15, 2000
REMED MALE DOTTED CONDOM PREVENTOR, LUCKY BOY, SUMMIT
K993405 · HIS
Obstetrics & Gynecology · 130d
Cleared Feb 15, 2000
REMED MALE RIBBED CONDOM PREVENTOR, LUCKY BOY SUMMIT
K993408 · HIS
Obstetrics & Gynecology · 130d
Cleared Feb 14, 2000
REMED MALE LATEX CONDOM (SUPER DUPER) PREVENTOR, LUCKY BOY, AND SUMMIT
K993390 · HIS
Obstetrics & Gynecology · 129d
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