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FDA 510(k)

LASAG MICRORUPTOR 2 ND:YAG OPHTH. LASER SYSTEM

K-Number: K885164 · 1989-01-10

ApplicantChiron Vision Corp.
Decision Date1989-01-10
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LASAG MICRORUPTOR 2 ND:YAG OPHTH. LASER SYSTEM 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 1989-01-10 under 510(k) number K885164. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LASAG MICRORUPTOR 2 ND:YAG OPHTH. LASER SYSTEM?

LASAG MICRORUPTOR 2 ND:YAG OPHTH. LASER SYSTEM is a medical device that received FDA 510(k) clearance on 1989-01-10. The listed applicant is Chiron Vision Corp.. The 510(k) number is K885164.

When did LASAG MICRORUPTOR 2 ND:YAG OPHTH. LASER SYSTEM receive FDA 510(k) clearance?

LASAG MICRORUPTOR 2 ND:YAG OPHTH. LASER SYSTEM received FDA 510(k) clearance on 1989-01-10, under 510(k) number K885164.

Who is the listed applicant for LASAG MICRORUPTOR 2 ND:YAG OPHTH. LASER SYSTEM?

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 LASAG MICRORUPTOR 2 ND:YAG OPHTH. LASER SYSTEM?

The FDA product code for LASAG MICRORUPTOR 2 ND:YAG OPHTH. LASER SYSTEM is HQF.

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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.

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