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

GEN. DIAG. CHROMOSTRATE REF. PLASMA

K Number: K850409 · Decision May 8, 1985
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
180
Applicant Total
50
Review Days
93

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Basic Information

Device Name
GEN. DIAG. CHROMOSTRATE REF. PLASMA
K Number
K850409
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5425
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Warner-Lambert Co.
Date Received
February 4, 1985
Decision Date
May 8, 1985
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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