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FDA 510(k)

SLT LASERPRO CTH HOLMIUM LASER SYSTEM

K-Number: K011409 · 2001-06-14

ApplicantSurgical Laser Technologies, Inc.
Decision Date2001-06-14
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SLT LASERPRO CTH HOLMIUM LASER SYSTEM 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 2001-06-14 under 510(k) number K011409. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SLT LASERPRO CTH HOLMIUM LASER SYSTEM?

SLT LASERPRO CTH HOLMIUM LASER SYSTEM is a medical device that received FDA 510(k) clearance on 2001-06-14. The listed applicant is Surgical Laser Technologies, Inc.. The 510(k) number is K011409.

When did SLT LASERPRO CTH HOLMIUM LASER SYSTEM receive FDA 510(k) clearance?

SLT LASERPRO CTH HOLMIUM LASER SYSTEM received FDA 510(k) clearance on 2001-06-14, under 510(k) number K011409.

Who is the listed applicant for SLT LASERPRO CTH HOLMIUM LASER SYSTEM?

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 SLT LASERPRO CTH HOLMIUM LASER SYSTEM?

The FDA product code for SLT LASERPRO CTH HOLMIUM LASER SYSTEM is GEX. This falls under the Gastroenterology category.

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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: 0041-6772/0041-6781/0041-6752/0041-6761/0041-6912/0041-6921K010041SLT DIFFUSER FIBERK984018HEMOSLEEVE, MODEL 4.0MM, 5.5MMK983050PNEUMATIC CUTTER SYSTEMK981041SLT BIPOLAR SHEATH

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Related Devices (Code: GEX)

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.

K254199PicoreMax (PicoreMax)BLUECORE COMPANY Co., Ltd.K252723Dynamis Pro FamilyFotona D.O.O.K241973SmartIPL_NI SystemLumenis Be, Ltd.K261047Dental Diode Laser Device (Laser-Pen)Guilin Kevin Peter Technology Co., Ltd.K261817Diode Laser Therapy System (PZ-BDT67-01, PZ-BDT67-02)Zhengzhou PZ Laser Slim Technology Co., Ltd.K261673LED Therapy Device (QLXY-01)Beijing Nubway S&T Co., Ltd.

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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