Biotecx Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biotecx Laboratories, Inc. - FDA 510(k) Cleared Devices
15
Total
15
Cleared
0
Denied
Biotecx Laboratories, Inc. has 15 FDA 510(k) cleared chemistry devices. Based in Mchenry, US.
Historical record: 15 cleared submissions from 1978 to 1999.
Browse the complete list of FDA 510(k) cleared chemistry devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biotecx Laboratories, Inc.
15 devices
Cleared
Feb 03, 1999
OPTICOAT T4 EIA KIT
Chemistry
217d
Cleared
Dec 22, 1998
OPTICOAT T3 EIA KIT
Chemistry
214d
Cleared
Oct 19, 1989
CORTISOL CLASP-BEAD EIA KIT
Chemistry
43d
Cleared
Aug 11, 1989
T3 CLASP-BEAD EIA KIT
Chemistry
92d
Cleared
May 22, 1989
T4 CLASP-BEAD EIA KIT
Chemistry
34d
Cleared
Oct 31, 1988
TBG 125I RIA KIT, RADIOIMMUNO. OF SERUM THYROXINE
Chemistry
55d
Cleared
Apr 13, 1987
PROGESTERONE CLASP RADIOIMMUNOASSAY KIT
Chemistry
18d
Cleared
Sep 25, 1986
HPL RIA KIT
Chemistry
37d
Cleared
Mar 17, 1986
ALDOSTERONE DIRECT RIA KIT
Chemistry
101d
Cleared
Jun 06, 1985
ESTRADIOL DIRECT RIA KIT
Chemistry
51d
Cleared
Feb 01, 1985
RADIOIMMUNOASSAY OF HUMAN SERUM PLASMA OR URINE TO
Chemistry
56d
Cleared
Sep 14, 1984
CORITSOL PREMIX RIA KIT
Chemistry
49d
Cleared
Aug 07, 1984
DHEA-S DIRECT RIA KIT
Chemistry
36d
Cleared
May 02, 1984
PROGESTERONE DIRECT RIA KIT-RADIOIMM
Chemistry
30d
Cleared
Jun 30, 1978
ELECTRO-PLETHYSMOGRAPH
Cardiovascular
52d