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

MARQUETTE EAR PROBE SENSOR

K Number: K942752 · Decision Sep 2, 1994
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
10
Applicant Total
82
Review Days
84

Basic Information

Device Name
MARQUETTE EAR PROBE SENSOR
K Number
K942752
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2710
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MARQUETTE ELECTRONICS, INC.
Date Received
June 10, 1994
Decision Date
September 2, 1994
Product Code
DPZ
Advisory Committee
Cardiovascular
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DPZ Oximeter, Ear

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