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FDA 510(k)

SENTORR ARTERIAL PRESSURE SENSOR

K-Number: K880830 · 1988-08-12

ApplicantOhmeda Medical
Decision Date1988-08-12
Product CodeDXO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SENTORR ARTERIAL PRESSURE SENSOR is the device name listed in this FDA 510(k) record. The listed applicant is Ohmeda Medical. It received FDA 510(k) clearance on 1988-08-12 under 510(k) number K880830. The device is classified under product code DXO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SENTORR ARTERIAL PRESSURE SENSOR?

SENTORR ARTERIAL PRESSURE SENSOR is a medical device that received FDA 510(k) clearance on 1988-08-12. The listed applicant is Ohmeda Medical. The 510(k) number is K880830.

When did SENTORR ARTERIAL PRESSURE SENSOR receive FDA 510(k) clearance?

SENTORR ARTERIAL PRESSURE SENSOR received FDA 510(k) clearance on 1988-08-12, under 510(k) number K880830.

Who is the listed applicant for SENTORR ARTERIAL PRESSURE SENSOR?

The FDA 510(k) record lists Ohmeda Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SENTORR ARTERIAL PRESSURE SENSOR?

The FDA product code for SENTORR ARTERIAL PRESSURE SENSOR is DXO.

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Other records listing Ohmeda Medical as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K123309GIRAFFE AND PANDA WARMERSK101788GIRAFFE OMNIBEDK101778GIRAFFE INCUBATORK090697MODIFICATION TO: GIRAFFE AND PANDA WARMERK072157MODIFICATION TO GIRAFFE AND PANDA WARMERS (GIRAFFE AND PANDA UNINTERRUPTIBLE POWER SUPPLY)K070377GIRAFFE AND PANDA WARMER

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Related Devices (Code: DXO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K251367OptoMonitor 3Opsens, Inc.K241418OptoMonitor 3Opsens, Inc.K233904ACIST RXi System (016616); ACIST Navvus II Catheter (016675_Acist Medical Systems, Inc.K222216TruWave Disposable Pressure TransducerEdwards Lifesciences, LLCK202943OptoMonitor 3Opsens, Inc.K193620OptoMonitor 3Opsens, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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