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FDA 510(k)

MOTHER'S MILK BAG

K-Number: K874071 · 1987-12-08

Decision Date1987-12-08
Product CodeHGX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MOTHER'S MILK BAG is the device name listed in this FDA 510(k) record. The listed applicant is Yanase Waitch K.K.. It received FDA 510(k) clearance on 1987-12-08 under 510(k) number K874071. 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 MOTHER'S MILK BAG?

MOTHER'S MILK BAG is a medical device that received FDA 510(k) clearance on 1987-12-08. The listed applicant is Yanase Waitch K.K.. The 510(k) number is K874071.

When did MOTHER'S MILK BAG receive FDA 510(k) clearance?

MOTHER'S MILK BAG received FDA 510(k) clearance on 1987-12-08, under 510(k) number K874071.

Who is the listed applicant for MOTHER'S MILK BAG?

The FDA 510(k) record lists Yanase Waitch K.K. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MOTHER'S MILK BAG?

The FDA product code for MOTHER'S MILK BAG is HGX.

Related Clinical Trials

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.

Related Devices (Code: HGX)

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.

Official Source

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