R. K. Medical L. L. C. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
R. K. Medical L. L. C. - FDA 510(k) Cleared Devices
5
Total
1
Cleared
0
Denied
R. K. Medical L. L. C. has 1 FDA 510(k) cleared medical devices. Based in Mahwah, US.
Historical record: 1 cleared submissions from 1996 to 1996. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by R. K. Medical L. L. C. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - R. K. Medical L. L. C.
5 devices
Cleared
Jul 29, 1996
POLYESTER NONABSORBABLE SURGICAL SUTURES USP
General & Plastic Surgery
73d
Cleared
Jul 29, 1996
PLAIN GUT & CHRONIC GUT ABSORBABLE SURGICAL SUTURES USP
General & Plastic Surgery
73d
Cleared
Jun 18, 1996
POLYPROPYLENE NONABSORBABLE SURGICAL SUTURES
General & Plastic Surgery
69d
Cleared
Mar 04, 1996
NYLON NOABSORBABLE SURGICAL SUTURES USP
General & Plastic Surgery
40d
Cleared
Mar 04, 1996
SILK NONABSORBABLE SURGICAL SUTURES USP
General & Plastic Surgery
40d