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FDA 510(k)

MOMO DESIGN OR MOMO

K-Number: K972416 · 1997-07-21

ApplicantMomo U.S.A., Inc.
Decision Date1997-07-21
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MOMO DESIGN OR MOMO is the device name listed in this FDA 510(k) record. The listed applicant is Momo U.S.A., Inc.. It received FDA 510(k) clearance on 1997-07-21 under 510(k) number K972416. The device is classified under product code HQY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOMO DESIGN OR MOMO?

MOMO DESIGN OR MOMO is a medical device that received FDA 510(k) clearance on 1997-07-21. The listed applicant is Momo U.S.A., Inc.. The 510(k) number is K972416.

When did MOMO DESIGN OR MOMO receive FDA 510(k) clearance?

MOMO DESIGN OR MOMO received FDA 510(k) clearance on 1997-07-21, under 510(k) number K972416.

Who is the listed applicant for MOMO DESIGN OR MOMO?

The FDA 510(k) record lists Momo U.S.A., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MOMO DESIGN OR MOMO?

The FDA product code for MOMO DESIGN OR MOMO is HQY.

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Related Devices (Code: HQY)

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.

K974852NON-PRESCRIPTION SUNGLASSESChia Hui Spectacles Mfg. Corp.K974860NON-PRESCRIPTION SUNGLASSESWenzhou Ming Ming Optical Co. , Ltd.K974861NON-PRESCRIPTION SUNGLASSESWenzhou Hindar Optical Co., Ltd.K974511SUNGLASSESSun World Intl., Inc.K974441SUNGLASSESHip Shing Fat Co., Ltd.K973528SUNGLASSESJeou Jeou Long Industrial Co., Ltd.

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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