Atlas FDA

VENOUS OXYGEN PROBE

FDA 510(k) clearance K811071 · decided 1981-05-05

Clearance details

K-number
K811071
Device name
VENOUS OXYGEN PROBE
Applicant
G.D. Searle and Co.
Decision
Substantially Equivalent
Date received
1981-04-20
Decision date
1981-05-05
Days to decision
15 days
Clearance type
Traditional
Product code
CCE
Device class
2
Regulation number
868.1200
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
Location
Walker, MI, 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
VIA 1-01 INFUSION PUMP/BLOOD CHEMISTRY SYSTEM (K935778)Via Medical Corp.1996-12-05
SYSTEM ATHENA-PRODUCT ENHANCEMENTS, ANESTHESIA (K912145)S & W Medico Teknik1992-05-05
TOPS NEEDLE TIP PROBE & PVC TIP PROBE (K910453)Baxter Healthcare Corp1991-08-13
PB3200 INTRA-ARTERIAL BLOOD GAS MONITORING SYSTEM (K905397)Puritan Bennett Corp.1991-05-14
OPTEX BLOOD GAS MONITORING SYSTEM (K896311)Optex Biomedical1990-01-03
TISSUE OXYGEN MONITOR SYSTEM, MODEL II (K890624)Baxter Healthcare Corp1989-12-22
NEOCATH 1000 UMBILICAL ARTERY OXYGEN MONITORING SY (K895149)Shiley, Inc.1989-11-28
CONTINUCATH 1000 INTRAVASCULAR OXYGEN MONITORING (K895150)Shiley, Inc.1989-11-28
BARD ABG 100 INTRAVASCULAR OXYGEN MONITOR SYSTEM (K884063)C.R. Bard, Inc.1988-12-16
UMBILICAL ARTERY OXYGEN SENSOR (K875225)Ohmeda Medical1988-03-04
UMBILICAL ARTERY OXYGEN PROBE MODEL UAP-100 (K872896)American Bentley1988-02-12
BARD ABG 100 INTRAVASCULAR OXYGEN MONITOR. SYSTEM (K872125)C.R. Bard, Inc.1987-12-11

Recalls involving this device

No recalls on record reference this clearance.