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

ADVIA CENTAUR CALIBRATOR 30, MODELS 10379811/10379810

K Number: K100293 · Decision Mar 19, 2010
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
244
Applicant Total
3
Review Days
45

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
ADVIA CENTAUR CALIBRATOR 30, MODELS 10379811/10379810
K Number
K100293
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
862.1150
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Siemens Heatlhcare Diagnostics, Inc.
Date Received
February 2, 2010
Decision Date
March 19, 2010
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 Siemens Heatlhcare Diagnostics, Inc.

K Number Device Name
K102772 DIMENSION MYCOPHENOLIC ACID (MPAT) FLEX REAGENT CARTRIDGE, DIMENSION MYCOPHENOLIC ACID CALIBRATOR (MPAT CAL)
K102045 DIMENSION VISA HBA1C, MODEL K3105A