FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

EMBLETTA MPR

K Number: K122516 · Decision Feb 21, 2013
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
155
Applicant Total
4
Review Days
188

Basic Information

Device Name
EMBLETTA MPR
K Number
K122516
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2375
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
EMBLA SYSTEMS
Date Received
August 17, 2012
Decision Date
February 21, 2013
Product Code
MNR
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
MNR Ventilatory Effort Recorder

Similar 510(k) Clearances

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

View all

Other Clearances by EMBLA SYSTEMS

K Number Device Name
K162140 RemLogic
K153353 SANDMAN ELITE
K111742 MDRIVE