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FDA 510(k)

MICRORUPTOR III SYST, Q-SWITCHED ND:YAG LASER COMP

K-Number: K895864 · 1989-12-29

ApplicantLasag AG
Decision Date1989-12-29
Product CodeLXS
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MICRORUPTOR III SYST, Q-SWITCHED ND:YAG LASER COMP is the device name listed in this FDA 510(k) record. The listed applicant is Lasag AG. It received FDA 510(k) clearance on 1989-12-29 under 510(k) number K895864. The device is classified under product code LXS. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRORUPTOR III SYST, Q-SWITCHED ND:YAG LASER COMP?

MICRORUPTOR III SYST, Q-SWITCHED ND:YAG LASER COMP is a medical device that received FDA 510(k) clearance on 1989-12-29. The listed applicant is Lasag AG. The 510(k) number is K895864.

When did MICRORUPTOR III SYST, Q-SWITCHED ND:YAG LASER COMP receive FDA 510(k) clearance?

MICRORUPTOR III SYST, Q-SWITCHED ND:YAG LASER COMP received FDA 510(k) clearance on 1989-12-29, under 510(k) number K895864.

Who is the listed applicant for MICRORUPTOR III SYST, Q-SWITCHED ND:YAG LASER COMP?

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

What is the FDA product code for MICRORUPTOR III SYST, Q-SWITCHED ND:YAG LASER COMP?

The FDA product code for MICRORUPTOR III SYST, Q-SWITCHED ND:YAG LASER COMP is LXS.

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_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Lasag AG 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.

K900199LASAG MICRORUPTER 2 ND:YAG LASER TRABECULOPLASTY

Related Devices (Code: LXS)

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.

K023045MICRORUPTER VMeridian AGK901605PHOENIX LASER SYSTEMS OPHTHALMIC SURGICAL WORKSTA.Phoenix Laser Systems, Inc.K893987NIDEK MODEL YC-1200Nidek, Inc.K892204NIDEK INC. MODELS YC-2000 & 3000 OPHTHALMIC LASERSNidek, Inc.K892058ISL QC 2000Intelligent Surgical Lasers, Inc.

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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