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FDA 510(k)

ACUSON PHYSIOLOGICAL CONTROL MODULE

K-Number: K871239 · 1987-06-05

ApplicantAcuson Computed Sonography
Decision Date1987-06-05
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ACUSON PHYSIOLOGICAL CONTROL MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Acuson Computed Sonography. It received FDA 510(k) clearance on 1987-06-05 under 510(k) number K871239. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACUSON PHYSIOLOGICAL CONTROL MODULE?

ACUSON PHYSIOLOGICAL CONTROL MODULE is a medical device that received FDA 510(k) clearance on 1987-06-05. The listed applicant is Acuson Computed Sonography. The 510(k) number is K871239.

When did ACUSON PHYSIOLOGICAL CONTROL MODULE receive FDA 510(k) clearance?

ACUSON PHYSIOLOGICAL CONTROL MODULE received FDA 510(k) clearance on 1987-06-05, under 510(k) number K871239.

Who is the listed applicant for ACUSON PHYSIOLOGICAL CONTROL MODULE?

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

What is the FDA product code for ACUSON PHYSIOLOGICAL CONTROL MODULE?

The FDA product code for ACUSON PHYSIOLOGICAL CONTROL MODULE is DPS.

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Other records listing Acuson Computed Sonography 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.

K893863ACUSON L538 TRANSDUCERK874028ACUSON S328 TRANSDUCERK874861ACUSON S328 TRANSDUCER FOR CARDIAC COLOR FLOW APP.K874363ACUSON S228 AND S328 TRANSDUCERS FOR ABDOM. APPLI.K874922ACUSON TRANSPERINEAL NEEDLE GUIDEK874860ACUSON I7505 TRANSDUCER FOR INTRACAVITARY APPLICA.

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Related Devices (Code: DPS)

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.

K254255S-Patch CardioAIWellysis Corp.K252463SE-1202 Series Electrocardiograph (Model: SE-1202, SE-1202E)Edan Instruments, Inc.K251670MAC 7 Resting ECG Analysis SystemGe Medical Systems Information Technologies, Inc.K252361AccurECG Analysis System (v2.0)Accurkardia, Inc.K252474Withings BeamO (SCT02)WithingsK250569Cardiologs Holter PlatformPhilips France Commercial

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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