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FDA 510(k)

SLT CL60 CONTACT LASER SYSTEM, CUTTING & COAGULA.

K-Number: K882908 · 1988-09-30

ApplicantSurgical Laser Technologies, Inc.
Decision Date1988-09-30
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SLT CL60 CONTACT LASER SYSTEM, CUTTING & COAGULA. 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 1988-09-30 under 510(k) number K882908. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SLT CL60 CONTACT LASER SYSTEM, CUTTING & COAGULA.?

SLT CL60 CONTACT LASER SYSTEM, CUTTING & COAGULA. is a medical device that received FDA 510(k) clearance on 1988-09-30. The listed applicant is Surgical Laser Technologies, Inc.. The 510(k) number is K882908.

When did SLT CL60 CONTACT LASER SYSTEM, CUTTING & COAGULA. receive FDA 510(k) clearance?

SLT CL60 CONTACT LASER SYSTEM, CUTTING & COAGULA. received FDA 510(k) clearance on 1988-09-30, under 510(k) number K882908.

Who is the listed applicant for SLT CL60 CONTACT LASER SYSTEM, CUTTING & COAGULA.?

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 CL60 CONTACT LASER SYSTEM, CUTTING & COAGULA.?

The FDA product code for SLT CL60 CONTACT LASER SYSTEM, CUTTING & COAGULA. is HQF.

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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: HQF)

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.

K252979Voyager DSLT (430840610)Belkin Vision, Ltd.K251507INTEGRE LIOQuantel MedicalK251772Navilas Laser System 577sl (156691)Od-Os GmbHK243014EyeQ nanoECPEyeq, Inc.K240615Leos Laser and Endoscopy SystemBeaver-Visitec International, Inc.K242397LYNX PhotocoagulatorNorlase Aps

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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