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

MAGNESIUM TEST KIT

K Number: K803088 · Decision Jan 2, 1981
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
89
Applicant Total
92
Review Days
25

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Basic Information

Device Name
MAGNESIUM TEST KIT
K Number
K803088
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1495
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Mallinckrodt Critical Care
Date Received
December 8, 1980
Decision Date
January 2, 1981
Product Code
JGJ
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
JGJ Photometric Method, Magnesium

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Other Clearances by Mallinckrodt Critical Care

K Number Device Name
K880343 BURNEY GALLBLADDER CATHETER KIT
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K874514 HI-LO TEMP(R) GENERAL PURPOSE TEMPERATURE PROBE
K874568 HI-LO TEMP(R) MODEL 8700 PATIENT TEMP MONITOR
K874404 HI-LO TEMP(R) SKIN TEMPERATURE SENSOR
K873461 LASER-FLEX(TM) TRACHEAL TUBE (CUFFED)
K873833 THERMOCOUPLE ADAPTER
K873004 GUIDING CATHETER
K871204 CUFFED TRACHEAL TUBE (MULTIPLE)
K862666 UNCUFFED LASER RESISTEANT TRACHEAL TUBE(TENTATIVE)
Search all 92 clearances from Mallinckrodt Critical Care →