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

SPECTRO C

K Number: K872941 · Decision Sep 4, 1987
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
189
Applicant Total
9
Review Days
39

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Basic Information

Device Name
SPECTRO C
K Number
K872941
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7290
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Ramco Laboratories, Inc.
Date Received
July 27, 1987
Decision Date
September 4, 1987
Product Code
GGP
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
GGP Test, Qualitative And Quantitative Factor Deficiency

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Other Clearances by Ramco Laboratories, Inc.

K Number Device Name
K983107 VFE
K981208 TFR
K910481 EPO-RIA
K864701 VWF IMMUNOBLOT
K861159 SPECTRO VWF
K831470 PTH MR
K823016 CANDIDA DETECTION SYSTEM
K812056 SPECTRO FEIRITIN