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FDA 510(k)

ND:YAG SURGICAL LASER FOR ENDO. GASTRO/URO. APPLI.

K-Number: K874255 · 1988-07-12

ApplicantMinnesota Laser Corp.
Decision Date1988-07-12
Product CodeLNK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ND:YAG SURGICAL LASER FOR ENDO. GASTRO/URO. APPLI. 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 1988-07-12 under 510(k) number K874255. 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 ND:YAG SURGICAL LASER FOR ENDO. GASTRO/URO. APPLI.?

ND:YAG SURGICAL LASER FOR ENDO. GASTRO/URO. APPLI. is a medical device that received FDA 510(k) clearance on 1988-07-12. The listed applicant is Minnesota Laser Corp.. The 510(k) number is K874255.

When did ND:YAG SURGICAL LASER FOR ENDO. GASTRO/URO. APPLI. receive FDA 510(k) clearance?

ND:YAG SURGICAL LASER FOR ENDO. GASTRO/URO. APPLI. received FDA 510(k) clearance on 1988-07-12, under 510(k) number K874255.

Who is the listed applicant for ND:YAG SURGICAL LASER FOR ENDO. GASTRO/URO. APPLI.?

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 ENDO. GASTRO/URO. APPLI.?

The FDA product code for ND:YAG SURGICAL LASER FOR ENDO. GASTRO/URO. APPLI. is LNK.

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.

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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.

K874253ND:YAG SURGICAL LASER FOR GASTRO/UROLOGY APPLICA.K874254ND:YAG SURGICAL LASER FOR PULMONARY APPLICATIONSK854473PORTALASE 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: 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.K874253ND:YAG SURGICAL LASER FOR GASTRO/UROLOGY APPLICA.Minnesota Laser Corp.K880193MODEL 4060 N ND:YAG LASER FOR UROLOGICAL USESharplan Lasers, Inc.K880256MODEL 4060 N ND:YAG LASER FOR GASTROENTEROLOGY USESharplan Lasers, Inc.K875039ND:YAG 100 SURGICAL LASER FOR GASTRO. AND UROLOGYSurgilase, 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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