FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

BOTTLE BREATHING DEVICE

K Number: K780558 · Decision May 26, 1978
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
3
Applicant Total
18
Review Days
51

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Basic Information

Device Name
BOTTLE BREATHING DEVICE
K Number
K780558
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5220
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
B & F Medical Products, Inc.
Date Received
April 5, 1978
Decision Date
May 26, 1978
Product Code
BYO
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
BYO Bottle, Blow

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Other Clearances by B & F Medical Products, Inc.

K Number Device Name
K942645 B&F MEDICAL OXYGEN REG MECICAL OXY COMPRESS GAS REG
K920573 CANNULA NASAL OXYGEN
K913501 TRACHEOSTOMY MASK
K861325 MAXI-USE O2 DEVICE
K861054 DISPOSABLE RESCUE BREATHING DEVICE
K853004 PORTABLE OXYGEN UNIT
K843691 PORTABLE OXYGEN UNIT
K823532 STOCK #64091-PEDIATRIC OXYGEN MASK
K811404 TRAVELAIRE
K802644 EMERG. OXYGEN KIT #65350 & #65399 CASE
Search all 18 clearances from B & F Medical Products, Inc. →