Techhnilab Instruments, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Techhnilab Instruments, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Techhnilab Instruments, Inc. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1977 to 1981.
Browse the FDA 510(k) cleared devices submitted by Techhnilab Instruments, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Techhnilab Instruments, Inc.
6 devices
Cleared
Dec 31, 1981
ELECTRIC SELF STERILIZATION INOCUL. LOOP
Toxicology
15d
Cleared
May 26, 1978
THERMAJUST CIRCU-TEMP
Chemistry
53d
Cleared
Apr 24, 1978
DISC-PAK ROTATOR
Hematology
21d
Cleared
Aug 22, 1977
MULTI-CAVITY EQUILIBRIUM CELL
Chemistry
21d
Cleared
Jan 28, 1977
BEESON AUTOMADDAK FEEDER
Physical Medicine
3d
Cleared
Jan 28, 1977
MADDATHERM PARAFFIN BATH
Physical Medicine
3d