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

AQUALITE INTACT PTH

K Number: K970483 · Decision Apr 14, 1997
Classifications
1
FEI Numbers
43
Registration Numbers
43
Same Product Code
85
Applicant Total
11
Review Days
63

Basic Information

Device Name
AQUALITE INTACT PTH
K Number
K970483
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1545
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SEALITE SCIENCES, INC.
Date Received
February 10, 1997
Decision Date
April 14, 1997
Product Code
CEW
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
CEW Radioimmunoassay, Parathyroid Hormone

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