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

BIRD 1000 PV PORTABLE VENTILATOR

K Number: K925422 · Decision May 13, 1993
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
2
Applicant Total
35
Review Days
198

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
BIRD 1000 PV PORTABLE VENTILATOR
K Number
K925422
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Bird Products Corp.
Date Received
October 27, 1992
Decision Date
May 13, 1993
Product Code
CBC
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CBC Bottle, Collection And Trap, Breathing System (Uncalibrated)

Similar 510(k) Clearances

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

View all

Other Clearances by Bird Products Corp.

K Number Device Name
K032451 BIRD TBIRD VELA VENTILATOR
K022674 BIRD AVEA VENTILATOR
K013642 AVEA
K020730 ORION NASAL CPAP SYSTEM
K020746 BIRD TBIRD VELA VENTILATOR
K003770 BIRD TBIRD LEGACY VENTILATOR
K990856 HERITAGE NASAL CPAP SYSTEM, MODEL P/N 15682
K993449 BIRD V.I.P. GOLD/STERLING
K982580 BIRD MONITOR INTERFACE
K981971 TBIRD VS/AVS VOLUME VENTILATOR, MODELS 15568, 15570 , LP10 VOLUME VENTILATOR WITH PRESSURE LIMIT MODEL 00-004130, BEAR 3
Search all 35 clearances from Bird Products Corp. →