Atlas FDA

TRACHEOSTOMY MASK

FDA 510(k) clearance K913501 · decided 1992-01-13

Clearance details

K-number
K913501
Device name
TRACHEOSTOMY MASK
Applicant
B & F Medical Products, Inc.
Decision
Substantially Equivalent
Date received
1991-08-07
Decision date
1992-01-13
Days to decision
159 days
Clearance type
Traditional
Product code
BYG
Device class
1
Regulation number
868.5580
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
Location
Toledo, OH, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
FIRST AID KIT(S) (K963298)Vector, Inc.1996-11-06
HANS RUDOLPH NASAL CPAP MASK (K962848)Hans Rudolph, Inc.1996-10-16
DISPOSABLE, CPAP OXYGEN MASK (K945482)Fvtnks1995-09-19
WESTMED PEDIATRIC & ADULT MEDIUM CONCENTRATION OXYGEN MASK (K953464)Westmed, Inc.1995-09-18
VARIOUS ADULT & CHILD HIGH CON/NONREBREATH OXY MASKS (K953039)Dadsun Corp., Ltd.1995-09-15
WESTMED PEDIATRIC AND ADULT AEROSOL MASK (K945472)Westmed Intl.1995-02-07
JEMSDAL MASK (K942907)Respan Products, Inc.1994-08-31
SYSTEM 22 ADULT MASK (K940887)Medic-Aid , Ltd.1994-04-19
SYSTEM 22 PAEDIATRIC MASK (K940888)Medic-Aid , Ltd.1994-04-19
MEDWAY OXYGEN MASK (K931952)Medway1993-08-20
SURGICO OXYGEN MASK (K924069)Gujarat Surgico, Ltd.1993-02-04
SEAL RING FOR NASAL CPAP (K921499)Devilbiss Health Care, Inc.1992-09-17

Recalls involving this device

No recalls on record reference this clearance.