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

SECONDARY CALIBRATORS

K Number: K904698 · Decision Nov 28, 1990
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
244
Applicant Total
49
Review Days
43

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
SECONDARY CALIBRATORS
K Number
K904698
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1150
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Bionostics, Inc.
Date Received
October 16, 1990
Decision Date
November 28, 1990
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 Bionostics, Inc.

K Number Device Name
K131136 GLUCOSE METER-CHECK SOLUTION FOR TAIDOC
K123851 GLUCOSE METER-CHECK SOLUTION FOR ROCHE ACCU-CHEK
K123966 GLUCOSE METER-CHECK SOLUTION FOR BAYER
K113764 GLUCOSE METER-CHECK SOLUTION FOR INFOPIA
K112352 GLUCOSE METER-CHECK CONTROL FOR NIPRO TRUERESULT
K112356 GLUCOSE METER-CHECK CONTROL SOLUTION FOR AGAMATRIX WAVESENSE
K103553 LIFESCAN ONETOUCH SELECT / ULTRA / VITA GLUCOSE CONTROL SOLUTION
K101831 ENTERIX INSUREFIT FOB CONTROLS, MODEL 16800
K091914 OMNIS HEALTH EMBRACE GLUCOSE CONTROL SOLUTION
K081478 RNA MEDICAL GLUCOSE AND B-KETONE CALIBRATION VERIFICATION CONTROLS
Search all 49 clearances from Bionostics, Inc. →