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

LOFLO C5 CO2 SENSOR

K Number: K053174 · Decision Jan 12, 2006
Classifications
1
FEI Numbers
217
Registration Numbers
217
Same Product Code
304
Applicant Total
4
Review Days
59

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
LOFLO C5 CO2 SENSOR
K Number
K053174
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
868.1400
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Respironics Novametrix, LLC
Date Received
November 14, 2005
Decision Date
January 12, 2006
Product Code
CCK
Advisory Committee
Anesthesiology
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
CCK Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CCK), ordered by most recent decision date.

View all

Other Clearances by Respironics Novametrix, LLC

K Number Device Name
K103578 PHILIPS NM3 RESPIRATORY MONITOR WITH VENTASSIST
K091459 PHILIPS NM3 MONITOR, MODEL 7900
K080652 MERCURY VCO2 MODULE WITH CAPNOSTAT 5