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FDA 510(k)

HUNTLEIGH FETAL DOPPLER, FD-1 & DOPCORD, D140

K-Number: K900618 · 1990-04-25

ApplicantHuntleigh Technology, Inc.
Decision Date1990-04-25
Product CodeKNG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

HUNTLEIGH FETAL DOPPLER, FD-1 & DOPCORD, D140 is the device name listed in this FDA 510(k) record. The listed applicant is Huntleigh Technology, Inc.. It received FDA 510(k) clearance on 1990-04-25 under 510(k) number K900618. The device is classified under product code KNG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HUNTLEIGH FETAL DOPPLER, FD-1 & DOPCORD, D140?

HUNTLEIGH FETAL DOPPLER, FD-1 & DOPCORD, D140 is a medical device that received FDA 510(k) clearance on 1990-04-25. The listed applicant is Huntleigh Technology, Inc.. The 510(k) number is K900618.

When did HUNTLEIGH FETAL DOPPLER, FD-1 & DOPCORD, D140 receive FDA 510(k) clearance?

HUNTLEIGH FETAL DOPPLER, FD-1 & DOPCORD, D140 received FDA 510(k) clearance on 1990-04-25, under 510(k) number K900618.

Who is the listed applicant for HUNTLEIGH FETAL DOPPLER, FD-1 & DOPCORD, D140?

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

What is the FDA product code for HUNTLEIGH FETAL DOPPLER, FD-1 & DOPCORD, D140?

The FDA product code for HUNTLEIGH FETAL DOPPLER, FD-1 & DOPCORD, D140 is KNG.

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Other records listing Huntleigh Technology, Inc. as applicant

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Related Devices (Code: KNG)

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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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