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FDA 510(k)

SLT MULTIDIMENSIONAL CONTACT LASER SYST A4060C

K-Number: K930490 · 1993-03-31

ApplicantSurgical Laser Technologies, Inc.
Decision Date1993-03-31
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SLT MULTIDIMENSIONAL CONTACT LASER SYST A4060C 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 1993-03-31 under 510(k) number K930490. 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 MULTIDIMENSIONAL CONTACT LASER SYST A4060C?

SLT MULTIDIMENSIONAL CONTACT LASER SYST A4060C is a medical device that received FDA 510(k) clearance on 1993-03-31. The listed applicant is Surgical Laser Technologies, Inc.. The 510(k) number is K930490.

When did SLT MULTIDIMENSIONAL CONTACT LASER SYST A4060C receive FDA 510(k) clearance?

SLT MULTIDIMENSIONAL CONTACT LASER SYST A4060C received FDA 510(k) clearance on 1993-03-31, under 510(k) number K930490.

Who is the listed applicant for SLT MULTIDIMENSIONAL CONTACT LASER SYST A4060C?

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 MULTIDIMENSIONAL CONTACT LASER SYST A4060C?

The FDA product code for SLT MULTIDIMENSIONAL CONTACT LASER SYST A4060C 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: 0041-6772/0041-6781/0041-6752/0041-6761/0041-6912/0041-6921K011409SLT LASERPRO CTH HOLMIUM LASER SYSTEMK010041SLT DIFFUSER FIBERK984018HEMOSLEEVE, MODEL 4.0MM, 5.5MMK983050PNEUMATIC CUTTER SYSTEM

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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.

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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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