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

RESUSCITATION BAG CONTROLLER (RBC)

K Number: K882278 · Decision Jun 16, 1988
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
208
Applicant Total
8
Review Days
15

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Basic Information

Device Name
RESUSCITATION BAG CONTROLLER (RBC)
K Number
K882278
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5915
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Physician Engineered Products, Inc.
Date Received
June 1, 1988
Decision Date
June 16, 1988
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)

Similar 510(k) Clearances

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Other Clearances by Physician Engineered Products, Inc.

K Number Device Name
K110550 BRIGHT EMBRACE MODEL SBL60
K093618 BILI-MIRROR MODEL BLM-1
K974830 ULTRA BILI LIGHT
K883818 MODIFIED REFLUX REDUCER
K882291 RETROFIT BABY FACE SHIELD (RFS)
K873700 INSTITUTIONAL BILI LIGHT (IBL)
K850599 HOME BILI LIGHTS-MODEL 100