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FDA 510(k)

UNIMOM ALLEGRO

K-Number: K100929 · 2010-06-16

ApplicantBlue Egg CO
Decision Date2010-06-16
Product CodeHGX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

UNIMOM ALLEGRO is the device name listed in this FDA 510(k) record. The listed applicant is Blue Egg CO. It received FDA 510(k) clearance on 2010-06-16 under 510(k) number K100929. The device is classified under product code HGX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIMOM ALLEGRO?

UNIMOM ALLEGRO is a medical device that received FDA 510(k) clearance on 2010-06-16. The listed applicant is Blue Egg CO. The 510(k) number is K100929.

When did UNIMOM ALLEGRO receive FDA 510(k) clearance?

UNIMOM ALLEGRO received FDA 510(k) clearance on 2010-06-16, under 510(k) number K100929.

Who is the listed applicant for UNIMOM ALLEGRO?

The FDA 510(k) record lists Blue Egg CO as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UNIMOM ALLEGRO?

The FDA product code for UNIMOM ALLEGRO is HGX.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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