Atlas FDA

ARIZONA OXYGEN TIMER DEVICE

FDA 510(k) clearance K761260 · decided 1976-12-16

Clearance details

K-number
K761260
Device name
ARIZONA OXYGEN TIMER DEVICE
Applicant
The John Bunn Co.
Decision
Substantially Equivalent
Date received
1976-12-08
Decision date
1976-12-16
Days to decision
8 days
Clearance type
Traditional
Product code
BXP
Device class
1
Regulation number
868.2885
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
Location
Mchenry, IL, 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
UNIPOWER RECHARGEABLE BATTERY PACK (K936141)Unipower Corp.1994-03-31
TIMOX OXYGEN TIMER (K920360)Medical Fittings, Inc.1992-08-03
PHONATORY FUNCTION ANALYZER PS-77 (K832678)Kells Medical, Inc.1984-03-07
ULTRASONIC FLOWMETER (K800087)The Perkin-Elmer Corp.1980-03-19
OXY-ON DIGITAL OXYGEN TIMER (K781039)Chambers & Sadler Mfg.1978-08-31
OXYGEN TWMER, MODEL SST (K770424)Timeter Instrument Corp.1977-03-16

Recalls involving this device

No recalls on record reference this clearance.