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FDA 510(k)

DIGITAL BPM

K-Number: K790036 · 1979-03-02

ApplicantNarco Air-Shields
Decision Date1979-03-02
Product CodeDXO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DIGITAL BPM is the device name listed in this FDA 510(k) record. The listed applicant is Narco Air-Shields. It received FDA 510(k) clearance on 1979-03-02 under 510(k) number K790036. 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 DIGITAL BPM?

DIGITAL BPM is a medical device that received FDA 510(k) clearance on 1979-03-02. The listed applicant is Narco Air-Shields. The 510(k) number is K790036.

When did DIGITAL BPM receive FDA 510(k) clearance?

DIGITAL BPM received FDA 510(k) clearance on 1979-03-02, under 510(k) number K790036.

Who is the listed applicant for DIGITAL BPM?

The FDA 510(k) record lists Narco Air-Shields as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIGITAL BPM?

The FDA product code for DIGITAL BPM is DXO.

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Other records listing Narco Air-Shields 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.

K820114SYSTEM V.HEART RATE/RESPIR. RATE MONIT.K810953MODEL 533 PHOTOTHERAPY UNITK810474PROBE COVERK802800NARCO AIR-SHEILDS SYS. 100 MONITOR SYSK802126ISOLETTE INCUBATOR C-100K792592AMBU UNIVERSAL SUCTION PUMP

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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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