Medical Device Manufacturer · US , Mchenry , IL

Union Carbide Corp. - FDA 510(k) Cleared Devices

69 submissions · 69 cleared · Since 1976

Total

Cleared

Denied

Union Carbide Corp. has 69 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 69 cleared submissions from 1976 to 1983. Primary specialty: Chemistry.

Browse the FDA 510(k) cleared devices submitted by Union Carbide Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Union Carbide Corp.

69 devices

1-12 of 69

Cleared Mar 17, 1983

MARK III OXYGEN WALKER SYS-LOW PRESS

K830337 · BYJ

Anesthesiology · 44d

Cleared Apr 15, 1982

MARK III OXYGEN WALKER SYSTEM

LINDE MARK II OXYGEN RESERV. TYPE OR-4

K810732 · BYJ

Anesthesiology · 10d

Cleared Mar 17, 1981

CENTRIFI CHEM SYSTEM 400 ANALYZER

K810596 · JJE

Chemistry · 11d

Cleared Feb 02, 1981

CENTRIFICHEM SYSTEM 500

K810129 · JJE

Chemistry · 14d

Cleared Jan 09, 1981

CENTRIFICHEM AST/SGOT OPTIMIZED REAGENT

K803216 · CIT

Chemistry · 22d

Cleared Dec 10, 1980

CENTRIFICHEM COMB. SERUM-BASED CALIB.

K802741 · JIX

Chemistry · 37d

Cleared Nov 12, 1980

CENTRIFICHEM PIPETTOR ACCURACY CALIB.

K802520 · JQW

Chemistry · 28d

Cleared Oct 31, 1980

CENTRIFICHEM INORGANIC PHOSPHORUS

Looking for a specific device from Union Carbide Corp.? Search by device name or K-number.

Search all Union Carbide Corp. devices

Union Carbide Corp. - FDA 510(k) Cleared Devices

Filters