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

THYROID STIMULATING HORMONE METHOD

K Number: K970393 · Decision Mar 3, 1997
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
241
Applicant Total
13
Review Days
28

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Basic Information

Device Name
THYROID STIMULATING HORMONE METHOD
K Number
K970393
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1690
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dade Chemistry Systems, Inc.
Date Received
February 3, 1997
Decision Date
March 3, 1997
Product Code
JLW
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
JLW Radioimmunoassay, Thyroid-Stimulating Hormone

Similar 510(k) Clearances

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Other Clearances by Dade Chemistry Systems, Inc.

K Number Device Name
K973650 TROPONIN (TROP) METHOD
K973100 PROSTATE SPECIFIC ANTIGEN (PSA) CALIBRATOR
K973099 PROSTATE SPECIFIC ANTIGEN CONTROL
K973101 PROSTATE SPECIFIC ANTIGEN METHOD
K971141 FT4 METHOD FOR THE DIMENSION RXL CLINICAL CHEMISTRY SYSTEM
K970387 HUMAN CHORIONIC GONADOTROPIN METHOD
K970336 MMB CALIBRATOR
K970396 HUMAN CHORIONIC GONADOTROPIN CALIBRATOR
K970389 THYROID CALIBRATOR
K970343 MMB METHOD
Search all 13 clearances from Dade Chemistry Systems, Inc. →