FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

SEALITE SCIENCES, INC. AQUALITE PROLACTIN

K Number: K970188 · Decision Feb 20, 1997
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
79
Applicant Total
11
Review Days
34

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Basic Information

Device Name
SEALITE SCIENCES, INC. AQUALITE PROLACTIN
K Number
K970188
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1625
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sealite Sciences, Inc.
Date Received
January 17, 1997
Decision Date
February 20, 1997
Product Code
CFT
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CFT Radioimmunoassay, Prolactin (Lactogen)

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Other Clearances by Sealite Sciences, Inc.

K Number Device Name
K974551 SEALITE SCIENCES, INC. AQUALITE FREE T, ASSAY
K972761 SEALITE SCIENCES, INC. AQUALITE HUMAN GROWTH HORMONE ASSAY
K970612 SEALITE SCIENCES, INC. AQUALITE FERRITIN ASSAY
K970483 AQUALITE INTACT PTH
K970085 SEALITE SCIENCES AQUALITE FSH
K964925 SEALITE SCIENCES, INC. AQUALITE LH
K942661 AQUALITE TSH BIOLUMINESCENT IMMUNOASSAY KIT
K943437 AQUALITE FSH
K943188 SEALITE SCIENCE, INC. AQUALITE(R) LH
K941983 SEALITE SCIENCES INC.
Search all 11 clearances from Sealite Sciences, Inc. →