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FDA 510(k)

MATERNITY SUPPORTER

K-Number: K770162 · 1977-02-09

ApplicantR.G. Moore
Decision Date1977-02-09
Product CodeFSD
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MATERNITY SUPPORTER is the device name listed in this FDA 510(k) record. The listed applicant is R.G. Moore. It received FDA 510(k) clearance on 1977-02-09 under 510(k) number K770162. The device is classified under product code FSD. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MATERNITY SUPPORTER?

MATERNITY SUPPORTER is a medical device that received FDA 510(k) clearance on 1977-02-09. The listed applicant is R.G. Moore. The 510(k) number is K770162.

When did MATERNITY SUPPORTER receive FDA 510(k) clearance?

MATERNITY SUPPORTER received FDA 510(k) clearance on 1977-02-09, under 510(k) number K770162.

Who is the listed applicant for MATERNITY SUPPORTER?

The FDA 510(k) record lists R.G. Moore as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MATERNITY SUPPORTER?

The FDA product code for MATERNITY SUPPORTER is FSD.

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Related Devices (Code: FSD)

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.

K892379THE POUCH GROIN & ABDOMINAL STRESS AIDKuhn IndustriesK822817DOCE ALL-IN-THE-EAR AIDFidelty Hearing Instruments, Inc.K810379EARETTE HEARING AID SEARS #8054Oticon Corp.K760772DISPOSABLE ABDOMINAL BINDERTecnol New Jersey Wound Care, Inc.

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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