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FDA 510(k)

SLT CONTACT LASER SYSTEM CYCLOPHOTOCOAGULATION

K-Number: K882679 · 1988-12-14

ApplicantSurgical Laser Technologies, Inc.
Decision Date1988-12-14
Product CodeHQB
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SLT CONTACT LASER SYSTEM CYCLOPHOTOCOAGULATION 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 1988-12-14 under 510(k) number K882679. The device is classified under product code HQB. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SLT CONTACT LASER SYSTEM CYCLOPHOTOCOAGULATION?

SLT CONTACT LASER SYSTEM CYCLOPHOTOCOAGULATION is a medical device that received FDA 510(k) clearance on 1988-12-14. The listed applicant is Surgical Laser Technologies, Inc.. The 510(k) number is K882679.

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

SLT CONTACT LASER SYSTEM CYCLOPHOTOCOAGULATION received FDA 510(k) clearance on 1988-12-14, under 510(k) number K882679.

Who is the listed applicant for SLT CONTACT LASER SYSTEM CYCLOPHOTOCOAGULATION?

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 CONTACT LASER SYSTEM CYCLOPHOTOCOAGULATION?

The FDA product code for SLT CONTACT LASER SYSTEM CYCLOPHOTOCOAGULATION is HQB.

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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: HQB)

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.

K220263Vortex Surgical Laser Probes, Vortex Surgical Illuminated Laser Probes, Vortex Surgical Endoilluminators, Vortex Surgical ChandeliersVortex Surgical, Inc.K191846MAXReach Laser ProbeVortex Surgical, Inc.K182646Vitreq disposable laser probes, light fibers and ChandelierVitreQ BVK132614PEREGRINE CURVED ILLUMINATING LASER PROBEPeregrine Surgical , Ltd.K12299723GA CURVED ILLUMINATING LASER PROBEPeregrine Surgical , Ltd.K122905PEREGRINE 23GA CURVED LASER PROBEPeregrine Surgical , 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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