FDA 510(k)

POSTOPERATIVE UV GLASSES (PLANO/APHAKIC)

K-Number: K802651 · 1980-12-17

Decision Date1980-12-17

Product CodeHQG

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

POSTOPERATIVE UV GLASSES (PLANO/APHAKIC) is the device name listed in this FDA 510(k) record. The listed applicant is Chiron Vision Corp.. It received FDA 510(k) clearance on 1980-12-17 under 510(k) number K802651. 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 POSTOPERATIVE UV GLASSES (PLANO/APHAKIC)?

POSTOPERATIVE UV GLASSES (PLANO/APHAKIC) is a medical device that received FDA 510(k) clearance on 1980-12-17. The listed applicant is Chiron Vision Corp.. The 510(k) number is K802651.

When did POSTOPERATIVE UV GLASSES (PLANO/APHAKIC) receive FDA 510(k) clearance?

POSTOPERATIVE UV GLASSES (PLANO/APHAKIC) received FDA 510(k) clearance on 1980-12-17, under 510(k) number K802651.

Who is the listed applicant for POSTOPERATIVE UV GLASSES (PLANO/APHAKIC)?

The FDA 510(k) record lists Chiron Vision Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POSTOPERATIVE UV GLASSES (PLANO/APHAKIC)?

The FDA product code for POSTOPERATIVE UV GLASSES (PLANO/APHAKIC) is HQG.

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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.