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FDA 510(k)

ND:YAG SURGICAL LASER FOR PULMONARY APPLICATIONS

K-Number: K874254 · 1988-03-04

ApplicantMinnesota Laser Corp.
Decision Date1988-03-04
Product CodeLLO
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ND:YAG SURGICAL LASER FOR PULMONARY APPLICATIONS is the device name listed in this FDA 510(k) record. The listed applicant is Minnesota Laser Corp.. It received FDA 510(k) clearance on 1988-03-04 under 510(k) number K874254. The device is classified under product code LLO. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ND:YAG SURGICAL LASER FOR PULMONARY APPLICATIONS?

ND:YAG SURGICAL LASER FOR PULMONARY APPLICATIONS is a medical device that received FDA 510(k) clearance on 1988-03-04. The listed applicant is Minnesota Laser Corp.. The 510(k) number is K874254.

When did ND:YAG SURGICAL LASER FOR PULMONARY APPLICATIONS receive FDA 510(k) clearance?

ND:YAG SURGICAL LASER FOR PULMONARY APPLICATIONS received FDA 510(k) clearance on 1988-03-04, under 510(k) number K874254.

Who is the listed applicant for ND:YAG SURGICAL LASER FOR PULMONARY APPLICATIONS?

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

What is the FDA product code for ND:YAG SURGICAL LASER FOR PULMONARY APPLICATIONS?

The FDA product code for ND:YAG SURGICAL LASER FOR PULMONARY APPLICATIONS is LLO.

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 Minnesota Laser 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.

K874255ND:YAG SURGICAL LASER FOR ENDO. GASTRO/URO. APPLI.K874253ND:YAG SURGICAL LASER FOR GASTRO/UROLOGY APPLICA.K854473PORTALASE 300 CARBON DIOXIDE SURG LASER NEUROLOGICK854468PORTALASE 200 CARBON DIOXIDE SURG LASER NEUROLOGICK854471PORTALASE 300 CARBON DIOXIDE SURG LASER EAR/NOSE/TK854469PORTALASE 200 CARBON DIOXIDE SURG LASER DERMATOLOG

View all 12 devices →

Related Devices (Code: LLO)

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.

K884815SLT CLMD CONTACT LASERSurgical Laser Technologies, Inc.K881499SURGILASE YAG 100 FOR GYNECOLOGY USESurgilase, Inc.K880592LASEGUIDE 600A, 600B, 400A, 400B FOR PULMONARY USELaser Peripherals, LLCK880170MODEL 4900 ND:YAG LASER FOR PULMONARY OBSTRUCTIONSCooper Lasersonics, Inc.K875104SURGI-LIGHT DISPOSABLE SYSTEM FOR PULMONOLOGY USELaserguideK871876MODEL 5050 SURGILASER FOR PULMONARY USELasermatic, Inc.

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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