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FDA 510(k)

LASER PHOTOCOAGULATOR ARGON MED. LASER

K-Number: K813429 · 1982-01-22

ApplicantAmerican Laser Corp.
Decision Date1982-01-22
Product CodeHPJ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LASER PHOTOCOAGULATOR ARGON MED. LASER is the device name listed in this FDA 510(k) record. The listed applicant is American Laser Corp.. It received FDA 510(k) clearance on 1982-01-22 under 510(k) number K813429. The device is classified under product code HPJ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LASER PHOTOCOAGULATOR ARGON MED. LASER?

LASER PHOTOCOAGULATOR ARGON MED. LASER is a medical device that received FDA 510(k) clearance on 1982-01-22. The listed applicant is American Laser Corp.. The 510(k) number is K813429.

When did LASER PHOTOCOAGULATOR ARGON MED. LASER receive FDA 510(k) clearance?

LASER PHOTOCOAGULATOR ARGON MED. LASER received FDA 510(k) clearance on 1982-01-22, under 510(k) number K813429.

Who is the listed applicant for LASER PHOTOCOAGULATOR ARGON MED. LASER?

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

What is the FDA product code for LASER PHOTOCOAGULATOR ARGON MED. LASER?

The FDA product code for LASER PHOTOCOAGULATOR ARGON MED. LASER is HPJ.

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 American 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.

K010046NUVOLASE 532 MEDICAL LASER SYSTEMK990665BQ/BM INTEGRATED LASER DELIVERY SYSTEMK990725NUVOLASE 532 LASER SYSTEMK827819LASER PHOTOCOAGULATOR

Related Devices (Code: HPJ)

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.

K864012IRAS PERIMETERRandwal Instrument Co., Inc.K853556LASER IRASRandwal Instrument Co., Inc.K822415THE OCUPLOT DCoherent Medical DivisionK781507RETINOMETERCoburn Optical Ind., 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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