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FDA 510(k)

S.L.T. CONTACT LASER

K-Number: K855119 · 1986-02-24

ApplicantSurgical Laser Technologies, Inc.
Decision Date1986-02-24
Product CodeLNK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

S.L.T. CONTACT LASER is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Laser Technologies, Inc.. It received FDA 510(k) clearance on 1986-02-24 under 510(k) number K855119. 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 S.L.T. CONTACT LASER?

S.L.T. CONTACT LASER is a medical device that received FDA 510(k) clearance on 1986-02-24. The listed applicant is Surgical Laser Technologies, Inc.. The 510(k) number is K855119.

When did S.L.T. CONTACT LASER receive FDA 510(k) clearance?

S.L.T. CONTACT LASER received FDA 510(k) clearance on 1986-02-24, under 510(k) number K855119.

Who is the listed applicant for S.L.T. CONTACT LASER?

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

What is the FDA product code for S.L.T. CONTACT LASER?

The FDA product code for S.L.T. CONTACT LASER is LNK.

Related Clinical Trials

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Other records listing Surgical Laser Technologies, 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.

K042211MODIFICATION TO: LASERPRO 810, 940, AND 980 DIODE DIODE LASER SYSTEMSK023624SLT VENOUS FIBER DELIVERY SYSTEMS, MODEL: 0041-6772/0041-6781/0041-6752/0041-6761/0041-6912/0041-6921K011409SLT LASERPRO CTH HOLMIUM LASER SYSTEMK010041SLT DIFFUSER FIBERK984018HEMOSLEEVE, MODEL 4.0MM, 5.5MMK983050PNEUMATIC CUTTER SYSTEM

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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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