FDA 510(k)

LASERMED OCULASE ARGON LASER

K-Number: K828583 · 1983-01-14

Decision Date1983-01-14

Product Code

DecisionSubstantially Equivalent

Device Summary

LASERMED OCULASE 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 1983-01-14 under 510(k) number K828583. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LASERMED OCULASE ARGON LASER?

LASERMED OCULASE ARGON LASER is a medical device that received FDA 510(k) clearance on 1983-01-14. The listed applicant is Lasermed Corp.. The 510(k) number is K828583.

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

LASERMED OCULASE ARGON LASER received FDA 510(k) clearance on 1983-01-14, under 510(k) number K828583.

Who is the listed applicant for LASERMED OCULASE ARGON LASER?

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

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Lasermed Corp. as applicant

K843594AIRVIT MODEL 8500 K833532OCULASE 514 OPHTHALMIC ARGON LASER

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.