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FDA 510(k)

SLT CLMD CONTACT LASER

K-Number: K884815 · 1988-12-22

ApplicantSurgical Laser Technologies, Inc.
Decision Date1988-12-22
Product CodeLLO
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

SLT CLMD 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 1988-12-22 under 510(k) number K884815. The device is classified under product code LLO. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SLT CLMD CONTACT LASER?

SLT CLMD CONTACT LASER is a medical device that received FDA 510(k) clearance on 1988-12-22. The listed applicant is Surgical Laser Technologies, Inc.. The 510(k) number is K884815.

When did SLT CLMD CONTACT LASER receive FDA 510(k) clearance?

SLT CLMD CONTACT LASER received FDA 510(k) clearance on 1988-12-22, under 510(k) number K884815.

Who is the listed applicant for SLT CLMD 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 SLT CLMD CONTACT LASER?

The FDA product code for SLT CLMD CONTACT LASER is LLO.

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: LLO)

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.

K881499SURGILASE YAG 100 FOR GYNECOLOGY USESurgilase, Inc.K880592LASEGUIDE 600A, 600B, 400A, 400B FOR PULMONARY USELaser Peripherals, LLCK880170MODEL 4900 ND:YAG LASER FOR PULMONARY OBSTRUCTIONSCooper Lasersonics, Inc.K874254ND:YAG SURGICAL LASER FOR PULMONARY APPLICATIONSMinnesota Laser Corp.K875104SURGI-LIGHT DISPOSABLE SYSTEM FOR PULMONOLOGY USELaserguideK871876MODEL 5050 SURGILASER FOR PULMONARY USELasermatic, 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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