Bhp Diagnostix, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bhp Diagnostix, Inc. - FDA 510(k) Cleared Devices
25
Total
25
Cleared
0
Denied
Bhp Diagnostix, Inc. has 25 FDA 510(k) cleared chemistry devices. Based in Mchenry, US.
Historical record: 25 cleared submissions from 1978 to 1990.
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 - Bhp Diagnostix, Inc.
25 devices
Cleared
Nov 02, 1990
SERACON CR REFERENCE
Chemistry
31d
Cleared
Oct 29, 1986
SERACON CT REFERENCE
Chemistry
41d
Cleared
Aug 19, 1986
SERACON(TM) CAL (PRODUCT NO. DO35)
Chemistry
42d
Cleared
Mar 22, 1985
QUANTICEL HHR + TWO HUMAN HEMATOLOGY W/PLATELETS
Hematology
93d
Cleared
Mar 22, 1985
QUANTICEL HHR TWO HUMAN HEMATOLOGY REFERENCE
Hematology
93d
Cleared
Nov 27, 1984
SERACON TM SR IV
Chemistry
43d
Cleared
Nov 27, 1984
SERACON TM SR III
Chemistry
43d
Cleared
Dec 31, 1979
SERACON-SRI
Chemistry
28d
Cleared
Dec 31, 1979
SERACON-SRI (PROD. # D029
Chemistry
28d
Cleared
Dec 31, 1979
SERACON-SRII
Chemistry
28d
Cleared
Oct 17, 1979
SERACON - EL DO27
Chemistry
16d
Cleared
Oct 11, 1979
SERACON CAL D025
Chemistry
10d
Cleared
Oct 11, 1979
SERACON -LO DO26
Chemistry
10d
Cleared
Feb 26, 1979
SERACON-N
Chemistry
82d
Cleared
Feb 15, 1979
SERACON-LP
Chemistry
48d
Cleared
Feb 08, 1979
SERACON-A
Chemistry
64d
Cleared
Feb 08, 1979
SERACON-C
Chemistry
64d
Cleared
Feb 08, 1979
SERACON-HDL
Chemistry
41d
Cleared
Dec 04, 1978
SERACON-SRI
Chemistry
49d
Cleared
Dec 04, 1978
SERACON-SRII
Chemistry
49d
Cleared
Nov 15, 1978
QUANTICEL HHR, L531 AND L532
Hematology
26d
Cleared
Nov 15, 1978
QUANTICEL HHR # L500 AND L501
Hematology
27d
Cleared
Sep 14, 1978
QUANTICEL-HRP
Hematology
55d
Cleared
Jul 27, 1978
PLATELET CONTROL
Hematology
45d
Cleared
Jun 06, 1978
PLATELET CONTROL
Hematology
39d