FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

QUANTICEL HHR + TWO HUMAN HEMATOLOGY W/PLATELETS

K Number: K844927 · Decision Mar 22, 1985
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
191
Applicant Total
25
Review Days
93

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
QUANTICEL HHR + TWO HUMAN HEMATOLOGY W/PLATELETS
K Number
K844927
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.8625
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Bhp Diagnostix, Inc.
Date Received
December 19, 1984
Decision Date
March 22, 1985
Product Code
JPK
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JPK Mixture, Hematology Quality Control

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JPK), ordered by most recent decision date.

View all

Other Clearances by Bhp Diagnostix, Inc.

K Number Device Name
K904503 SERACON CR REFERENCE
K863648 SERACON CT REFERENCE
K862594 SERACON(TM) CAL (PRODUCT NO. DO35)
K844928 QUANTICEL HHR TWO HUMAN HEMATOLOGY REFERENCE
K844026 SERACON TM SR IV
K844027 SERACON TM SR III
K792486 SERACON-SRI (PROD. # D029
K792487 SERACON-SRII
K792485 SERACON-SRI
K791958 SERACON - EL DO27
Search all 25 clearances from Bhp Diagnostix, Inc. →