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

NPB-190 PULSE OXIMETER (NPB-190)

K Number: K971946 · Decision Aug 25, 1997
Classifications
1
FEI Numbers
403
Registration Numbers
403
Same Product Code
711
Applicant Total
42
Review Days
90

Basic Information

Device Name
NPB-190 PULSE OXIMETER (NPB-190)
K Number
K971946
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2700
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
NELLCOR PURITAN BENNETT, INC.
Date Received
May 27, 1997
Decision Date
August 25, 1997
Product Code
DQA
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
DQA Oximeter

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