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FDA 510(k)

SUN CLIP

K-Number: K961603 · 1996-05-13

ApplicantIntromark, Inc.
Decision Date1996-05-13
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SUN CLIP is the device name listed in this FDA 510(k) record. The listed applicant is Intromark, Inc.. It received FDA 510(k) clearance on 1996-05-13 under 510(k) number K961603. 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 SUN CLIP?

SUN CLIP is a medical device that received FDA 510(k) clearance on 1996-05-13. The listed applicant is Intromark, Inc.. The 510(k) number is K961603.

When did SUN CLIP receive FDA 510(k) clearance?

SUN CLIP received FDA 510(k) clearance on 1996-05-13, under 510(k) number K961603.

Who is the listed applicant for SUN CLIP?

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

What is the FDA product code for SUN CLIP?

The FDA product code for SUN CLIP is HQY.

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

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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