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FDA 510(k)

CORNING CPF 550 LENS

K-Number: K821398 · 1982-06-25

Decision Date1982-06-25
Product CodeHQG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CORNING CPF 550 LENS is the device name listed in this FDA 510(k) record. The listed applicant is Corning Medical & Scientific. It received FDA 510(k) clearance on 1982-06-25 under 510(k) number K821398. 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 CORNING CPF 550 LENS?

CORNING CPF 550 LENS is a medical device that received FDA 510(k) clearance on 1982-06-25. The listed applicant is Corning Medical & Scientific. The 510(k) number is K821398.

When did CORNING CPF 550 LENS receive FDA 510(k) clearance?

CORNING CPF 550 LENS received FDA 510(k) clearance on 1982-06-25, under 510(k) number K821398.

Who is the listed applicant for CORNING CPF 550 LENS?

The FDA 510(k) record lists Corning Medical & Scientific as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CORNING CPF 550 LENS?

The FDA product code for CORNING CPF 550 LENS 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.

Other records listing Corning Medical & Scientific as applicant

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.

View all 111 devices →

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

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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