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

DSL SOMATOMEDIN-C (DSL #5600)

K Number: K875229 · Decision Jul 1, 1988
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
35
Applicant Total
94
Review Days
192

Basic Information

Device Name
DSL SOMATOMEDIN-C (DSL #5600)
K Number
K875229
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1370
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
DIAGNOSTIC SYSTEMS LABORATORIES, INC.
Date Received
December 22, 1987
Decision Date
July 1, 1988
Product Code
CFL
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
CFL Radioimmunoassay, Human Growth Hormone

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