Biochem International, Inc. is one of 5787 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biochem International, Inc. - FDA 510(k) Cleared Devices
Recent clearances: BIOCHEM MODEL 3302 NEWOX2 OXIMETER, 8100 ANESTHETIC AGENT MONITOR, BIOCHEM 9100 MULTIGAS MONITOR IBP MODULE
28
Total
28
Cleared
0
Denied
Biochem International, Inc. has 28 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.
Historical record: 28 cleared submissions from 1977 to 1994.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biochem International, Inc.
28 devices
Cleared
Apr 11, 1994
BIOCHEM MODEL 3302 NEWOX2 OXIMETER
Anesthesiology
825d
Cleared
Dec 03, 1993
8100 ANESTHETIC AGENT MONITOR
Anesthesiology
200d
Cleared
May 26, 1993
BIOCHEM 9100 MULTIGAS MONITOR IBP MODULE
Cardiovascular
429d
Cleared
Jan 07, 1993
BIOCHEM MODEL 3301 NEWOX1 OXIMETER
Anesthesiology
366d
Cleared
Aug 22, 1991
BIOCHEM TEMPERATURE/ FIO2 MODULE
Anesthesiology
205d
Cleared
Aug 22, 1991
BIOCHEM 9100 MULTIGAS MONITOR TEMP/FIO1 MOD,NIBP
Cardiovascular
148d
Cleared
Sep 04, 1990
BIOCHEM 6100 NON-INVASIVE MONITOR
Cardiovascular
43d
Cleared
Jul 27, 1990
BIOCHEM 9100 MULTIGAS MONITOR
Anesthesiology
93d
Cleared
Dec 20, 1989
BIOCHEM 3100 OXIMETER
Cardiovascular
208d
Cleared
Aug 31, 1989
BIOCHEM 8100 ANESTHETIC AGENT MONITOR
Anesthesiology
141d
Cleared
Jun 15, 1989
BIOCHEM 520 BREATH INDICATOR
Anesthesiology
114d
Cleared
Dec 17, 1987
BIOCHEM 9090 CAPNOGRAPH/SAO2
Anesthesiology
86d