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

QUANTA PULSE OXIMETER, MODEL: PULSE LINK 1000 OR QH100

K Number: K083079 · Decision Mar 5, 2009
Classifications
1
FEI Numbers
400
Registration Numbers
400
Same Product Code
725
Applicant Total
5
Review Days
140

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Basic Information

Device Name
QUANTA PULSE OXIMETER, MODEL: PULSE LINK 1000 OR QH100
K Number
K083079
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2700
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Quanta Computer, Inc.
Date Received
October 16, 2008
Decision Date
March 5, 2009
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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