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FDA 510(k)

CHANGE IN FIBERLASE 100 ND:YAG MEDICAL LASER

K-Number: K863583 · 1986-11-24

ApplicantLaser Media
Decision Date1986-11-24
Product CodeLNK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CHANGE IN FIBERLASE 100 ND:YAG MEDICAL LASER is the device name listed in this FDA 510(k) record. The listed applicant is Laser Media. It received FDA 510(k) clearance on 1986-11-24 under 510(k) number K863583. The device is classified under product code LNK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHANGE IN FIBERLASE 100 ND:YAG MEDICAL LASER?

CHANGE IN FIBERLASE 100 ND:YAG MEDICAL LASER is a medical device that received FDA 510(k) clearance on 1986-11-24. The listed applicant is Laser Media. The 510(k) number is K863583.

When did CHANGE IN FIBERLASE 100 ND:YAG MEDICAL LASER receive FDA 510(k) clearance?

CHANGE IN FIBERLASE 100 ND:YAG MEDICAL LASER received FDA 510(k) clearance on 1986-11-24, under 510(k) number K863583.

Who is the listed applicant for CHANGE IN FIBERLASE 100 ND:YAG MEDICAL LASER?

The FDA 510(k) record lists Laser Media as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHANGE IN FIBERLASE 100 ND:YAG MEDICAL LASER?

The FDA product code for CHANGE IN FIBERLASE 100 ND:YAG MEDICAL LASER is LNK.

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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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Other records listing Laser Media 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.

K872352FIBERLASE II ND:YAG LASER FOR TREAT OF MENORRHAGIAK872351FIBERLASE II ND:YAG LASER FOR PULMONARY USEK872350FIBERLASE II ND:YAG LASER FOR GASTRO.&UROLOGY USEK872031UNI-FIBER NON-REPAIRABLE FIBER DELIVERY SYSTEMK863428SINGLE USE LASER FIBER DELIVERY SYSTEM FOR ND: YAGK862444FIBERLASE 100 MEDICAL LASER SYS/ND:YAG MENORRHAGIA

View all 12 devices →

Related Devices (Code: LNK)

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.

K925395TECHNOMED PULSOLITH 4000 LASER SYSTEMTeknomed, Inc.K901723MDL-2000 LASERTRIPTERCandela Laser Corp.K874255ND:YAG SURGICAL LASER FOR ENDO. GASTRO/URO. APPLI.Minnesota Laser Corp.K874253ND:YAG SURGICAL LASER FOR GASTRO/UROLOGY APPLICA.Minnesota Laser Corp.K880256MODEL 4060 N ND:YAG LASER FOR GASTROENTEROLOGY USESharplan Lasers, Inc.K880193MODEL 4060 N ND:YAG LASER FOR UROLOGICAL USESharplan Lasers, 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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