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FDA 510(k)

SEE MONSTERS SUNGLASSES

K-Number: K936218 · 1994-02-22

ApplicantDoppler, Inc.
Decision Date1994-02-22
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SEE MONSTERS SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Doppler, Inc.. It received FDA 510(k) clearance on 1994-02-22 under 510(k) number K936218. 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 SEE MONSTERS SUNGLASSES?

SEE MONSTERS SUNGLASSES is a medical device that received FDA 510(k) clearance on 1994-02-22. The listed applicant is Doppler, Inc.. The 510(k) number is K936218.

When did SEE MONSTERS SUNGLASSES receive FDA 510(k) clearance?

SEE MONSTERS SUNGLASSES received FDA 510(k) clearance on 1994-02-22, under 510(k) number K936218.

Who is the listed applicant for SEE MONSTERS SUNGLASSES?

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

What is the FDA product code for SEE MONSTERS SUNGLASSES?

The FDA product code for SEE MONSTERS SUNGLASSES 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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