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

FISHER DIAGNOSTICS SERA CHEM SMAC CALIBRATORS

K Number: K844047 · Decision Nov 9, 1984
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
244
Applicant Total
16
Review Days
23

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
FISHER DIAGNOSTICS SERA CHEM SMAC CALIBRATORS
K Number
K844047
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1150
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Fisher Diagnostics
Date Received
October 17, 1984
Decision Date
November 9, 1984
Product Code
JIT
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
JIT Calibrator, Secondary

Similar 510(k) Clearances

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

View all

Other Clearances by Fisher Diagnostics

K Number Device Name
K170652 ARCHITECT B.R.A.H.M.S PCT, ARCHITECT B.R.A.H.M.S PCT Calibrators, ARCHITECT B.R.A.H.M.S PCT Controls
K070640 ARCHITECT STAT TROPONIN-1; MYOGLOBIN
K052407 ARCHITECT ANTI-TPO IMMUNOASSAY, CALIBRATORS & CONTROLS
K052308 ARCHITECT ANTI-TG IMMUNOASSAY REAGENTS, CALIBRATORS, CONTROLS AND SYSTEM ASSAY CD-ROM
K042924 ARCHITECT STAT MYO IMMUNOASSAY
K041192 ARCHITECT STAT TROPONIN-I IMMUNOASSAY
K041596 ARCHITECT STAT CK-MB IMMUNOASSAY
K023362 FISHER DIAGNOSTICS THROMBOSCREEN 1000; PACIFIC HEMOSTASIS FIBRINOGEN REAGENT PLUS KAOLIN
K013397 PACIFIC HEMOSTASIS REFERENCE EMULSION
K010750 PACIFIC HEMOSTASIS INR CONTROL PLASMAS, MODEL CATALOG 100560
Search all 16 clearances from Fisher Diagnostics →