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

MACS CPAP SYSTEM

K Number: K080692 · Decision Jun 20, 2008
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
99
Applicant Total
4
Review Days
101

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
MACS CPAP SYSTEM
K Number
K080692
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5925
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Airon Corporation
Date Received
March 11, 2008
Decision Date
June 20, 2008
Product Code
BTL
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
BTL Ventilator, Emergency, Powered (Resuscitator)

Similar 510(k) Clearances

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

View all

Other Clearances by Airon Corporation

K Number Device Name
K121379 PNEUTON MINI VENTILATOR PNEUTON MINI NON-INVASIVE VENTILATION (NIV) KIT ACCESSORY
K043085 MODIFICATION TO: PNEUTON VENTILATOR
K024344 PNEUTON VENTILATOR