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

PH CALIBRATION BUFFERS

K Number: K772106 · Decision Dec 6, 1977
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
244
Applicant Total
39
Review Days
29

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Basic Information

Device Name
PH CALIBRATION BUFFERS
K Number
K772106
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1150
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
General Diagnostics
Date Received
November 7, 1977
Decision Date
December 6, 1977
Product Code
JIT
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
JIT Calibrator, Secondary

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