Atlas FDA

OXY-DIAL

FDA 510(k) clearance K852618 · decided 1985-09-18

Clearance details

K-number
K852618
Device name
OXY-DIAL
Applicant
Ashai Co. , Ltd.
Decision
Substantially Equivalent
Date received
1985-06-20
Decision date
1985-09-18
Days to decision
90 days
Clearance type
Traditional
Product code
BYF
Device class
1
Regulation number
868.5600
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
Location
Australia, AU
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
TRACH MASK MODEL (245, 246) (K955483)Hospitak, Inc.1996-02-28
VENTIMASK MK IV (K951652)Flexicare Medical, Ltd.1995-04-27
CARNATION TRACHEOSTOMY MASKS (K894457)Dadsun Corp., Ltd.1989-10-13
VENTURI MASK/ADULT & PAEDIATRIC (K860873)Dhd Medical Products Div. Diemolding Corp.1986-03-20
VENTURI MASK W/HUMDIFICATION CUP ADULT/PAEDIATRIC (K860874)Dhd Medical Products Div. Diemolding Corp.1986-03-19
DUAL DIAL VENTURI STYLE MASK (K832725)Airlife, Inc.1983-09-20
PERCENTO MASK, PEDIATRIC, UNDER-THE-CHIN (K812066)Airlife, Inc.1981-08-03
AIR ENTRAINMENT TRACH T (K810947)Airlife, Inc.1981-06-02
ADULT & PEDIATRIC TRACHEOSTOMY MASKS (K810946)Airlife, Inc.1981-06-02
VENTURI MASK/DELIVERY SYSTEM #'S (K810373)Todd Industries, Inc.1981-03-17
VENTURI MASK/DELIVERY SYSTEM #6078 (K810430)Todd Industries, Inc.1981-03-13
MASK, PERCENTO (K790146)Airlife, Inc.1979-02-06

Recalls involving this device

No recalls on record reference this clearance.