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FDA 510(k)

PLASTIC FRAME, METAL FRAME, OPTICAL

K-Number: K955695 · 1996-01-29

Decision Date1996-01-29
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PLASTIC FRAME, METAL FRAME, OPTICAL is the device name listed in this FDA 510(k) record. The listed applicant is Dah Sing Trading Co.. It received FDA 510(k) clearance on 1996-01-29 under 510(k) number K955695. 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 PLASTIC FRAME, METAL FRAME, OPTICAL?

PLASTIC FRAME, METAL FRAME, OPTICAL is a medical device that received FDA 510(k) clearance on 1996-01-29. The listed applicant is Dah Sing Trading Co.. The 510(k) number is K955695.

When did PLASTIC FRAME, METAL FRAME, OPTICAL receive FDA 510(k) clearance?

PLASTIC FRAME, METAL FRAME, OPTICAL received FDA 510(k) clearance on 1996-01-29, under 510(k) number K955695.

Who is the listed applicant for PLASTIC FRAME, METAL FRAME, OPTICAL?

The FDA 510(k) record lists Dah Sing Trading Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PLASTIC FRAME, METAL FRAME, OPTICAL?

The FDA product code for PLASTIC FRAME, METAL FRAME, OPTICAL 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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