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

DESTINY MAX COAGULATION ANALYZER

K Number: K083896 · Decision Jul 2, 2009
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
180
Applicant Total
5
Review Days
185

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Basic Information

Device Name
DESTINY MAX COAGULATION ANALYZER
K Number
K083896
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5425
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Trinity Biotech
Date Received
December 29, 2008
Decision Date
July 2, 2009
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 Trinity Biotech

K Number Device Name
K172254 Lyme B. burgdorferi (IgM) MarStripe Test
K163095 Lyme B. burgdorferi (IgG) MarStripe Test
K120001 UNIGOLD GIARDIA
K121565 UNI-GOLD CRYPTOSPORIDIUM