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FDA 510(k)

#6000 ND:YAG LASER SYSTEM UROLOGY/GASTROINTESTINAL

K-Number: K861903 · 1986-06-20

ApplicantCooper Lasersonics, Inc.
Decision Date1986-06-20
Product CodeLNK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

#6000 ND:YAG LASER SYSTEM UROLOGY/GASTROINTESTINAL 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 1986-06-20 under 510(k) number K861903. The device is classified under product code LNK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the #6000 ND:YAG LASER SYSTEM UROLOGY/GASTROINTESTINAL?

#6000 ND:YAG LASER SYSTEM UROLOGY/GASTROINTESTINAL is a medical device that received FDA 510(k) clearance on 1986-06-20. The listed applicant is Cooper Lasersonics, Inc.. The 510(k) number is K861903.

When did #6000 ND:YAG LASER SYSTEM UROLOGY/GASTROINTESTINAL receive FDA 510(k) clearance?

#6000 ND:YAG LASER SYSTEM UROLOGY/GASTROINTESTINAL received FDA 510(k) clearance on 1986-06-20, under 510(k) number K861903.

Who is the listed applicant for #6000 ND:YAG LASER SYSTEM UROLOGY/GASTROINTESTINAL?

The FDA 510(k) record lists Cooper Lasersonics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for #6000 ND:YAG LASER SYSTEM UROLOGY/GASTROINTESTINAL?

The FDA product code for #6000 ND:YAG LASER SYSTEM UROLOGY/GASTROINTESTINAL is LNK.

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Other records listing Cooper Lasersonics, Inc. as applicant

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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

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Related Devices (Code: LNK)

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.

K925395TECHNOMED PULSOLITH 4000 LASER SYSTEMTeknomed, Inc.K901723MDL-2000 LASERTRIPTERCandela Laser Corp.K874255ND:YAG SURGICAL LASER FOR ENDO. GASTRO/URO. APPLI.Minnesota Laser Corp.K874253ND:YAG SURGICAL LASER FOR GASTRO/UROLOGY APPLICA.Minnesota Laser Corp.K880256MODEL 4060 N ND:YAG LASER FOR GASTROENTEROLOGY USESharplan Lasers, Inc.K880193MODEL 4060 N ND:YAG LASER FOR UROLOGICAL USESharplan Lasers, 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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