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FDA 510(k)

SOLARSHIELD CLIPS

K-Number: K925531 · 1994-02-22

Decision Date1994-02-22
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SOLARSHIELD CLIPS is the device name listed in this FDA 510(k) record. The listed applicant is Dioptics Medical Products, Inc.. It received FDA 510(k) clearance on 1994-02-22 under 510(k) number K925531. 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 SOLARSHIELD CLIPS?

SOLARSHIELD CLIPS is a medical device that received FDA 510(k) clearance on 1994-02-22. The listed applicant is Dioptics Medical Products, Inc.. The 510(k) number is K925531.

When did SOLARSHIELD CLIPS receive FDA 510(k) clearance?

SOLARSHIELD CLIPS received FDA 510(k) clearance on 1994-02-22, under 510(k) number K925531.

Who is the listed applicant for SOLARSHIELD CLIPS?

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

What is the FDA product code for SOLARSHIELD CLIPS?

The FDA product code for SOLARSHIELD CLIPS is HQY.

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: 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.

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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