FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

CKMB/MYOGLOBIN MASS MEASUREMENY CONTROL LEVEL 1, 2, 3,

K Number: K944923 · Decision Nov 4, 1994
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
96
Applicant Total
17
Review Days
29

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
CKMB/MYOGLOBIN MASS MEASUREMENY CONTROL LEVEL 1, 2, 3,
K Number
K944923
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Clinical Controls, Inc.
Date Received
October 6, 1994
Decision Date
November 4, 1994
Product Code
JJT
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
JJT Enzyme Controls (Assayed And Unassayed)

Similar 510(k) Clearances

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

View all

Other Clearances by Clinical Controls, Inc.

K Number Device Name
K964278 WHOLE BLOOD GLUCOSE CONTROL LEVEL 1,2,AND 3/WHOLE BLOOD GLUCOSE LINEARITY CONTROL-LEVEL1,2,3,4,5,AND 6
K962432 LIQUISPEX URINE (MICRO)ALBUMIN CONTROL
K955690 AQUEOUS ETHANOL/AMMONIA CONTROL LEVEL 1, 2, & 3
K955691 SERUM VOLATILES CONTROL LEVEL 1 & 2
K946265 FIBRINOGEN HIGH ABNORMAL CONTROL - LEVEL 3
K935598 PLASMA FIBRINOGEN CONTROL LEVEL 1/LEVEL 2
K946049 LIQUISPEX(TM) LIQUID B2M/CRP CONTROL LEVEL 1 AND 2
K946048 LIQUISPEX(TM) LIQUID B2M CONTROL LEVEL 1 AND 2
K946050 LIQUISPEX(TM) LIQUID CRP CONTROL LEVEL 1 AND 2
K946266 FERRITIN CONTROL - LEVEL 1, 2, 3
Search all 17 clearances from Clinical Controls, Inc. →