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FDA 510(k)

MICROLASE BY LASER TRABECULOPLASTY

K-Number: K895213 · 1989-10-31

ApplicantKeeler Instruments, Inc.
Decision Date1989-10-31
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MICROLASE BY LASER TRABECULOPLASTY is the device name listed in this FDA 510(k) record. The listed applicant is Keeler Instruments, Inc.. It received FDA 510(k) clearance on 1989-10-31 under 510(k) number K895213. 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 MICROLASE BY LASER TRABECULOPLASTY?

MICROLASE BY LASER TRABECULOPLASTY is a medical device that received FDA 510(k) clearance on 1989-10-31. The listed applicant is Keeler Instruments, Inc.. The 510(k) number is K895213.

When did MICROLASE BY LASER TRABECULOPLASTY receive FDA 510(k) clearance?

MICROLASE BY LASER TRABECULOPLASTY received FDA 510(k) clearance on 1989-10-31, under 510(k) number K895213.

Who is the listed applicant for MICROLASE BY LASER TRABECULOPLASTY?

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

What is the FDA product code for MICROLASE BY LASER TRABECULOPLASTY?

The FDA product code for MICROLASE BY LASER TRABECULOPLASTY 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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