Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

COOPER LASERSONICS ND:YAG LASER 8000

K-Number: K841793 · 1984-06-07

ApplicantCooper Lasersonics, Inc.
Decision Date1984-06-07
Product Code
DecisionSubstantially Equivalent

Device Summary

COOPER LASERSONICS ND:YAG LASER 8000 is the device name listed in this FDA 510(k) record. The listed applicant is Cooper Lasersonics, Inc.. It received FDA 510(k) clearance on 1984-06-07 under 510(k) number K841793. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COOPER LASERSONICS ND:YAG LASER 8000?

COOPER LASERSONICS ND:YAG LASER 8000 is a medical device that received FDA 510(k) clearance on 1984-06-07. The listed applicant is Cooper Lasersonics, Inc.. The 510(k) number is K841793.

When did COOPER LASERSONICS ND:YAG LASER 8000 receive FDA 510(k) clearance?

COOPER LASERSONICS ND:YAG LASER 8000 received FDA 510(k) clearance on 1984-06-07, under 510(k) number K841793.

Who is the listed applicant for COOPER LASERSONICS ND:YAG LASER 8000?

The FDA 510(k) record lists Cooper Lasersonics, Inc. 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_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 Cooper Lasersonics, Inc. 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.

K880808ILLUMINA MODEL 40 CO2 LASER FOR GENERAL/PLASTIC SUK880807ILLUMINA MODEL 25 CO2 LASER FOR GENERAL/PLASTIC SUK880427ILLUMINA 40 CO2 LASER SYSTEMK880428ILLUMINA 25 CO2 LASER SYSTEMK880429ILLUMINA 55 CO2 LASER SYSTEMK880809ILLUMINA MODEL 55 CO2 LASER FOR GENERAL/PLASTIC SU

View all 54 devices →

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.

↑