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FDA 510(k)

OPHTHALMIC SPECTACLE LENS BLANKS

K-Number: K881225 · 1988-04-19

Decision Date1988-04-19
Product CodeHQG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OPHTHALMIC SPECTACLE LENS BLANKS is the device name listed in this FDA 510(k) record. The listed applicant is Beta Optical Co, Inc.. It received FDA 510(k) clearance on 1988-04-19 under 510(k) number K881225. The device is classified under product code HQG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPHTHALMIC SPECTACLE LENS BLANKS?

OPHTHALMIC SPECTACLE LENS BLANKS is a medical device that received FDA 510(k) clearance on 1988-04-19. The listed applicant is Beta Optical Co, Inc.. The 510(k) number is K881225.

When did OPHTHALMIC SPECTACLE LENS BLANKS receive FDA 510(k) clearance?

OPHTHALMIC SPECTACLE LENS BLANKS received FDA 510(k) clearance on 1988-04-19, under 510(k) number K881225.

Who is the listed applicant for OPHTHALMIC SPECTACLE LENS BLANKS?

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

What is the FDA product code for OPHTHALMIC SPECTACLE LENS BLANKS?

The FDA product code for OPHTHALMIC SPECTACLE LENS BLANKS is HQG.

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: HQG)

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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