Armkel, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Armkel, LLC - FDA 510(k) Cleared Devices
68
Total
68
Cleared
0
Denied
Armkel, LLC has 68 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 68 cleared submissions from 1979 to 2004. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Armkel, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Armkel, LLC
68 devices
Cleared
Oct 19, 2004
FIRST RESPONSE ONE-STEP DIGITAL PREGNANCY TEST
Chemistry
200d
Cleared
Feb 25, 2003
FIRST RESPONSE PREGNANCY TEST
Chemistry
32d
Cleared
Dec 16, 2002
TROJAN MINT TINGLE BRAND LATEX CONDOMS
Obstetrics & Gynecology
67d
Cleared
Mar 05, 2002
TROJAN PASSION BERRY GEL
Obstetrics & Gynecology
140d
Cleared
Feb 01, 2002
TROJAN CRYSTAL CLEAR LIQUID
Obstetrics & Gynecology
88d
Cleared
May 09, 2000
TROJAN EXTRA LARGE LATEX CONDOM
Obstetrics & Gynecology
25d
Cleared
Apr 06, 2000
TROJAN LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT
Obstetrics & Gynecology
29d
Cleared
Dec 21, 1999
FIRST RESPONSE 1-STEP PREGNANCY
Chemistry
172d
Cleared
Oct 27, 1997
TBD* ONE-STEP OVULATION PREDICTOR TEST
Chemistry
54d
Cleared
Oct 27, 1997
BRAND NAME *1-STEP PREGNANCY
Chemistry
52d
Cleared
Mar 03, 1997
LEGIONELLA IGG/IGM ELISA TEST SYSTEM
Microbiology
192d
Cleared
Feb 24, 1997
CHLAMYDIA IGG ELISA TEST SYSTEM
Microbiology
238d
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