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

INCENT-O-NEB

K Number: K781731 · Decision Dec 5, 1978
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
107
Applicant Total
18
Review Days
54

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Basic Information

Device Name
INCENT-O-NEB
K Number
K781731
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5690
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
B & F Medical Products, Inc.
Date Received
October 12, 1978
Decision Date
December 5, 1978
Product Code
BWF
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
BWF Spirometer, Therapeutic (Incentive)

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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. →