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

PHOTOMETER, SEROMETER (MODEL 380)

K Number: K760395 · Decision Nov 1, 1976
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
257
Applicant Total
92
Review Days
87

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Basic Information

Device Name
PHOTOMETER, SEROMETER (MODEL 380)
K Number
K760395
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2300
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Mallinckrodt Critical Care
Date Received
August 6, 1976
Decision Date
November 1, 1976
Product Code
JJQ
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
JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use

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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)
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