International Newtech Development, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
International Newtech Development, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
International Newtech Development, Inc. has 8 FDA 510(k) cleared medical devices. Based in Richmond, B.C., CA.
Historical record: 8 cleared submissions from 1995 to 2000. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by International Newtech Development, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - International Newtech Development, Inc.
8 devices
Cleared
Jan 03, 2000
URINALYSIS REAGENT STRIPS (10 PARAMETERS)
Chemistry
52d
Cleared
Apr 09, 1998
ONE STEP MIDSTREAM HCG PREGNANCY TEST
Chemistry
164d
Cleared
Apr 09, 1998
MINISTRIP/ SERUM AND URINE COMBO HCG TEST
Chemistry
164d
Cleared
Mar 13, 1998
PS-UNIT CASSETTE/SERUM AND URINE COMBO HCG
Chemistry
143d
Cleared
Feb 06, 1997
HCG CONTROLS
Chemistry
20d
Cleared
Nov 18, 1996
MINI STRIP/SERUM HCG
Chemistry
98d
Cleared
Nov 18, 1996
PS-UNIT CASSETTE/SERUM HCG
Chemistry
98d
Cleared
Oct 03, 1995
MINISTRIP HCG
Chemistry
172d