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

RESPIRONICS BAGEASY ENCOR ADULT SEMI-REUSABLE

K Number: K934699 · Decision Jan 5, 1995
Classifications
1
FEI Numbers
80
Registration Numbers
80
Same Product Code
207
Applicant Total
153
Review Days
462

Basic Information

Device Name
RESPIRONICS BAGEASY ENCOR ADULT SEMI-REUSABLE
K Number
K934699
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5915
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
RESPIRONICS, INC.
Date Received
September 30, 1993
Decision Date
January 5, 1995
Product Code
BTM
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
BTM Ventilator, Emergency, Manual (Resuscitator)

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