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FDA 510(k)

BF24 DOPPLER MODEL P872 AND P874

K-Number: K837481 · 1983-06-24

ApplicantMedasonics, Inc.
Decision Date1983-06-24
Product Code
DecisionSubstantially Equivalent

Device Summary

BF24 DOPPLER MODEL P872 AND P874 is the device name listed in this FDA 510(k) record. The listed applicant is Medasonics, Inc.. It received FDA 510(k) clearance on 1983-06-24 under 510(k) number K837481. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BF24 DOPPLER MODEL P872 AND P874?

BF24 DOPPLER MODEL P872 AND P874 is a medical device that received FDA 510(k) clearance on 1983-06-24. The listed applicant is Medasonics, Inc.. The 510(k) number is K837481.

When did BF24 DOPPLER MODEL P872 AND P874 receive FDA 510(k) clearance?

BF24 DOPPLER MODEL P872 AND P874 received FDA 510(k) clearance on 1983-06-24, under 510(k) number K837481.

Who is the listed applicant for BF24 DOPPLER MODEL P872 AND P874?

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

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Other records listing Medasonics, Inc. 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.

K991441CADENCE DOPPLER ULTRASOUND SYSTEMK962796NEUROGUARD TRANSCRANIAL DOPPLER ULTRASOUND SYSTEMK961116FIRST BEAT/CARDIO BEAT/CALCK914862CEREBROVASCULAR DIAGNOSTIC SYSTEM; CDSK911453OBTRASOUND STETHOSCOPE FETAL CALCK882018MEDACORD PVL, PERSONAL VASCULAR LABORATORY

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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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