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

NEOPLASTINE CI PLUS

K Number: K922040 · Decision Jun 23, 1992
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
126
Applicant Total
79
Review Days
53

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Basic Information

Device Name
NEOPLASTINE CI PLUS
K Number
K922040
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7750
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
American Bioproducts Co.
Date Received
May 1, 1992
Decision Date
June 23, 1992
Product Code
GJS
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
GJS Test, Time, Prothrombin

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