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FDA 510(k)

BABY DOPPLEX 4002-TWINS, MODEL BD4002

K-Number: K001882 · 2000-09-19

ApplicantHuntleigh Healthcare, Inc.
Decision Date2000-09-19
Product CodeHGM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

BABY DOPPLEX 4002-TWINS, MODEL BD4002 is the device name listed in this FDA 510(k) record. The listed applicant is Huntleigh Healthcare, Inc.. It received FDA 510(k) clearance on 2000-09-19 under 510(k) number K001882. The device is classified under product code HGM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BABY DOPPLEX 4002-TWINS, MODEL BD4002?

BABY DOPPLEX 4002-TWINS, MODEL BD4002 is a medical device that received FDA 510(k) clearance on 2000-09-19. The listed applicant is Huntleigh Healthcare, Inc.. The 510(k) number is K001882.

When did BABY DOPPLEX 4002-TWINS, MODEL BD4002 receive FDA 510(k) clearance?

BABY DOPPLEX 4002-TWINS, MODEL BD4002 received FDA 510(k) clearance on 2000-09-19, under 510(k) number K001882.

Who is the listed applicant for BABY DOPPLEX 4002-TWINS, MODEL BD4002?

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

What is the FDA product code for BABY DOPPLEX 4002-TWINS, MODEL BD4002?

The FDA product code for BABY DOPPLEX 4002-TWINS, MODEL BD4002 is HGM.

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Other records listing Huntleigh Healthcare, 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.

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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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