FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

STA(R) - LIQUID ANTI-XA, MULTI HEP CALIBRATOR, QUALITY HNF / UFH, QUALITY HBPM / LMWH

K Number: K111822 · Decision Oct 26, 2011
Classifications
1
FEI Numbers
10
Registration Numbers
10
Same Product Code
45
Applicant Total
16
Review Days
120

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
STA(R) - LIQUID ANTI-XA, MULTI HEP CALIBRATOR, QUALITY HNF / UFH, QUALITY HBPM / LMWH
K Number
K111822
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7525
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Diagnostica Stago, Inc.
Date Received
June 28, 2011
Decision Date
October 26, 2011
Product Code
KFF
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
KFF Assay, Heparin

Similar 510(k) Clearances

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

View all

Other Clearances by Diagnostica Stago, Inc.

K Number Device Name
K253658 STA Satellite Max®
K120014 STA- COAG CONTROL (N+ABN) PLUS
K092937 STA-HYBRID HEP CALIBRATOR
K093167 STA COMPACT AUTOMATED MULTI-PARAMETRIC ANALYZER
K092170 STA LIATEST FREE PS
K092113 STA - FREE PS CALIBRATOR
K082248 STA SATELLITE AUTOMATED MULTI-PARAMETER ANALYZER
K082675 STA-R EVOLUTION AUTOMATED MULTI-PARAMETRIC ANALYZER
K061805 STA - STACLOT DRVV SCREEN; STA - STACLOT DRVV CONFIRM
K061803 STA - CONTROL LA 1+2
Search all 16 clearances from Diagnostica Stago, Inc. →