Kendall Research Center - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Kendall Research Center has 14 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 14 cleared submissions from 1976 to 1980.
Browse the FDA 510(k) cleared devices submitted by Kendall Research Center Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kendall Research Center
14 devices
Cleared
Sep 26, 1980
TENDER-SORB DRAIN SPONGES
General & Plastic Surgery
14d
Cleared
Sep 20, 1978
T.E.D. SEQUENTIAL COMPRESSION SLEEVES
Cardiovascular
43d
Cleared
Mar 22, 1978
MICRONET LIGHT DRESSING SPONGE
General & Plastic Surgery
9d
Cleared
Feb 14, 1978
CATHETER/HEMOSTATIC/GERIATRIC
Gastroenterology & Urology
33d
Cleared
Feb 06, 1978
ANESTHESIA TRAY, CAUDAL
Anesthesiology
14d
Cleared
Nov 28, 1977
URINE SPECIMEN COLLECTING DEVICE
Gastroenterology & Urology
14d
Cleared
Nov 28, 1977
SYRINGE, IRRIGATION, PRE-FILLED
Gastroenterology & Urology
14d
Cleared
Oct 14, 1977
CURITY PEAKOMETER
Gastroenterology & Urology
46d
Cleared
Sep 15, 1977
CURITY IRRIGATION TRAY
General & Plastic Surgery
92d
Cleared
Sep 12, 1977
CONFORM STRETCH BANDAGE (5SIZES)
Physical Medicine
40d
Cleared
Sep 12, 1977
CONFORM ELASTIC NETTING
General Hospital
28d
Cleared
Aug 10, 1977
GREEN RADIOPAQUE IN SURG. SPONGES
General & Plastic Surgery
82d
Cleared
Aug 11, 1976
TRAY, CURITY CONTINUOUS EPIDURAL
Anesthesiology
12d
Cleared
Jul 16, 1976
SPONGE, CURITY WASHED GAUZE
General & Plastic Surgery
25d