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

MERCURY VCO2

K Number: K092217 · Decision Aug 21, 2009
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
60
Applicant Total
7
Review Days
30

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Basic Information

Device Name
MERCURY VCO2
K Number
K092217
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
868.1850
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Respironics Novametrix, Inc.
Date Received
July 22, 2009
Decision Date
August 21, 2009
Product Code
BZK
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
BZK Spirometer, Monitoring (W/Wo Alarm)

Similar 510(k) Clearances

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

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Other Clearances by Respironics Novametrix, Inc.

K Number Device Name
K042601 CAPNOSTAT 5
K032971 TIDAL WAVE SP MODEL 710/715 AND 715
K032949 SPOT CHECK PULSE OXIMETER,512/513
K041450 MODIFICATION TO NICO WITH MARS, MODEL 7300
K032755 MODEL 509M PULSE OXIMETER, MODEL 509M
K030886 NICO WITH MARS, MODEL 7300