FDA 510(k)

FETAL DOPPLER

K-Number: K905536 · 1992-04-21

ApplicantToshiba America Medical Systems, In.C

Decision Date1992-04-21

Product CodeMAA

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

FETAL DOPPLER is the device name listed in this FDA 510(k) record. The listed applicant is Toshiba America Medical Systems, In.C. It received FDA 510(k) clearance on 1992-04-21 under 510(k) number K905536. The device is classified under product code MAA. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FETAL DOPPLER?

FETAL DOPPLER is a medical device that received FDA 510(k) clearance on 1992-04-21. The listed applicant is Toshiba America Medical Systems, In.C. The 510(k) number is K905536.

When did FETAL DOPPLER receive FDA 510(k) clearance?

FETAL DOPPLER received FDA 510(k) clearance on 1992-04-21, under 510(k) number K905536.

Who is the listed applicant for FETAL DOPPLER?

The FDA 510(k) record lists Toshiba America Medical Systems, In.C as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FETAL DOPPLER?

The FDA product code for FETAL DOPPLER is MAA.

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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.