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

FINGER AND EAR SENSORS AND NEONATAL-ADULT AND ADULT/PEDIATRIC ADHESIVE SENSORS FOR USE WITH NELLCOR R-CAL SPO2

K Number: K061191 · Decision May 22, 2006
Classifications
1
FEI Numbers
400
Registration Numbers
400
Same Product Code
725
Applicant Total
2
Review Days
24

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Basic Information

Device Name
FINGER AND EAR SENSORS AND NEONATAL-ADULT AND ADULT/PEDIATRIC ADHESIVE SENSORS FOR USE WITH NELLCOR R-CAL SPO2
K Number
K061191
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.2700
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Measurement Specialties, Inc.
Date Received
April 28, 2006
Decision Date
May 22, 2006
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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Other Clearances by Measurement Specialties, Inc.

K Number Device Name
K010706 THINNER RESOLVE FITNESS MONITOR/BODY SCALE, HEALTH-O-METER