Allercare/Nsl, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Allercare/Nsl, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Allercare/Nsl, Inc. has 4 FDA 510(k) cleared medical devices. Based in Lincolnwood, US.
Historical record: 4 cleared submissions from 1990 to 1990. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Allercare/Nsl, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Allercare/Nsl, Inc.
4 devices
Cleared
May 16, 1990
LATEX CONDOMS - CODE NO. 401, 421 & 1002
Obstetrics & Gynecology
36d
Cleared
May 16, 1990
LATEX CONDOMS - CODE NO. 402, CODE NO. 1028
Obstetrics & Gynecology
36d
Cleared
May 16, 1990
LATEX CONDOMS - CODE NO. 404, NO. 424 & NO. 1000
Obstetrics & Gynecology
36d
Cleared
May 16, 1990
LATEX CONDOMS - CODE NO. 403, 406, 421 & 1033
Obstetrics & Gynecology
34d