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FDA 510(k)

JR -- OPHTHALMIC ARGON LASER

K-Number: K932296 · 1993-11-12

ApplicantCarson Laserworks
Decision Date1993-11-12
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

JR -- OPHTHALMIC ARGON LASER is the device name listed in this FDA 510(k) record. The listed applicant is Carson Laserworks. It received FDA 510(k) clearance on 1993-11-12 under 510(k) number K932296. 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 JR -- OPHTHALMIC ARGON LASER?

JR -- OPHTHALMIC ARGON LASER is a medical device that received FDA 510(k) clearance on 1993-11-12. The listed applicant is Carson Laserworks. The 510(k) number is K932296.

When did JR -- OPHTHALMIC ARGON LASER receive FDA 510(k) clearance?

JR -- OPHTHALMIC ARGON LASER received FDA 510(k) clearance on 1993-11-12, under 510(k) number K932296.

Who is the listed applicant for JR -- OPHTHALMIC ARGON LASER?

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

What is the FDA product code for JR -- OPHTHALMIC ARGON LASER?

The FDA product code for JR -- OPHTHALMIC ARGON LASER is HQF.

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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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