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

AEROSURE MEDIC

K Number: K140772 · Decision Dec 19, 2014
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
107
Applicant Total
7
Review Days
267

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
AEROSURE MEDIC
K Number
K140772
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5690
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Actegy , Ltd.
Date Received
March 27, 2014
Decision Date
December 19, 2014
Product Code
BWF
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
BWF Spirometer, Therapeutic (Incentive)

Similar 510(k) Clearances

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

View all

Other Clearances by Actegy , Ltd.

K Number Device Name
K210825 Revitive Medic Coach (Model Number 5575AQ)
K192887 Revitive Medic Plus, Revitive Advanced 2
K190924 Revitive Medic Plus, Revitive Advanced 2
K152480 Revitive Medic; Revitive MV; Revitive LV
K143207 Revitive IX (OTC)
K123354 REVITIVE IX