Andronic Devices, Ltd. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Andronic Devices, Ltd. - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Andronic Devices, Ltd. has 16 FDA 510(k) cleared medical devices. Based in Richmond,B.C. V6v-2j2, CA.
Historical record: 16 cleared submissions from 1987 to 1994. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Andronic Devices, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Andronic Devices, Ltd.
16 devices
Cleared
Nov 21, 1994
INSIGHT ELECTRONIC ALIGNMENT INDICATOR
Neurology
272d
Cleared
May 26, 1994
INSITE MODEL 20 & MODEL 15 INSUFFLATORS
Obstetrics & Gynecology
224d
Cleared
May 26, 1994
INSITE FILTER & TUBING SET
Obstetrics & Gynecology
224d
Cleared
Apr 15, 1994
KAPS POSITIONING ARM
General & Plastic Surgery
158d
Cleared
Apr 13, 1994
AUTOQUOT AUTOMATED ALIQUOTTING SYSTEM
Chemistry
231d
Cleared
Mar 31, 1994
ENDEX ENDOSCOPIC POSITIONING SYSTEM
General & Plastic Surgery
101d
Cleared
Feb 03, 1994
ARTHROBOT BI-FOLD DRAPE
General Hospital
269d
Cleared
Oct 19, 1992
ADEPT ENDOSCOPIC POSITIONER
General & Plastic Surgery
138d
Cleared
Oct 19, 1992
ADEPT INSTRUMENT POSITIONING ACCESSORY
General & Plastic Surgery
138d
Cleared
Aug 02, 1991
ARTHROBOT(TM) 75 (190 CM) GENERAL PURPOSE DRAPE
General Hospital
120d
Cleared
Aug 02, 1991
ARTHROBOT(TM) 96 (240 CM) DRAPE WITH 1 STRAP
General Hospital
120d
Cleared
Apr 29, 1991
ARTHROBOT(TM) WRIST HOLDER ACCESSORY
General & Plastic Surgery
25d