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FDA 510(k)

OCULASE 514 OPHTHALMIC ARGON LASER

K-Number: K833532 · 1984-02-04

ApplicantLasermed Corp.
Decision Date1984-02-04
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OCULASE 514 OPHTHALMIC ARGON LASER is the device name listed in this FDA 510(k) record. The listed applicant is Lasermed Corp.. It received FDA 510(k) clearance on 1984-02-04 under 510(k) number K833532. 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 OCULASE 514 OPHTHALMIC ARGON LASER?

OCULASE 514 OPHTHALMIC ARGON LASER is a medical device that received FDA 510(k) clearance on 1984-02-04. The listed applicant is Lasermed Corp.. The 510(k) number is K833532.

When did OCULASE 514 OPHTHALMIC ARGON LASER receive FDA 510(k) clearance?

OCULASE 514 OPHTHALMIC ARGON LASER received FDA 510(k) clearance on 1984-02-04, under 510(k) number K833532.

Who is the listed applicant for OCULASE 514 OPHTHALMIC ARGON LASER?

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

What is the FDA product code for OCULASE 514 OPHTHALMIC ARGON LASER?

The FDA product code for OCULASE 514 OPHTHALMIC ARGON LASER is HQF.

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.

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Other records listing Lasermed Corp. 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.

K843594AIRVIT MODEL 8500K828583LASERMED OCULASE ARGON LASER

Related Devices (Code: HQF)

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.

K252979Voyager DSLT (430840610)Belkin Vision, Ltd.K251507INTEGRE LIOQuantel MedicalK251772Navilas Laser System 577sl (156691)Od-Os GmbHK243014EyeQ nanoECPEyeq, Inc.K240615Leos Laser and Endoscopy SystemBeaver-Visitec International, Inc.K242397LYNX PhotocoagulatorNorlase Aps

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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