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

RIA-DAC TM HTSH KIH

K Number: K770604 · Decision Apr 6, 1977
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
241
Applicant Total
92
Review Days
6

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Basic Information

Device Name
RIA-DAC TM HTSH KIH
K Number
K770604
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1690
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Mallinckrodt Critical Care
Date Received
March 31, 1977
Decision Date
April 6, 1977
Product Code
JLW
Advisory Committee
Clinical Chemistry
Review Advisory Committee
IM
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

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K873461 LASER-FLEX(TM) TRACHEAL TUBE (CUFFED)
K873833 THERMOCOUPLE ADAPTER
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K871204 CUFFED TRACHEAL TUBE (MULTIPLE)
K862666 UNCUFFED LASER RESISTEANT TRACHEAL TUBE(TENTATIVE)
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