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

STA Satellite Max®

K Number: K253658 · Decision Apr 27, 2026
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
180
Applicant Total
16
Review Days
158

Basic Information

Device Name
STA Satellite Max®
K Number
K253658
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5425
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Diagnostica Stago, Inc.
Date Received
November 20, 2025
Decision Date
April 27, 2026
Product Code
JPA
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
JPA System, Multipurpose For In Vitro Coagulation Studies

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Other Clearances by Diagnostica Stago, Inc.

K Number Device Name
K120014 STA- COAG CONTROL (N+ABN) PLUS
K111822 STA(R) - LIQUID ANTI-XA, MULTI HEP CALIBRATOR, QUALITY HNF / UFH, QUALITY HBPM / LMWH
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. →