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FDA 510(k)

FIBERLASE II ND:YAG LASER FOR PULMONARY USE

K-Number: K872351 · 1987-12-11

ApplicantLaser Media
Decision Date1987-12-11
Product CodeLLO
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

FIBERLASE II ND:YAG LASER FOR PULMONARY USE is the device name listed in this FDA 510(k) record. The listed applicant is Laser Media. It received FDA 510(k) clearance on 1987-12-11 under 510(k) number K872351. 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 FIBERLASE II ND:YAG LASER FOR PULMONARY USE?

FIBERLASE II ND:YAG LASER FOR PULMONARY USE is a medical device that received FDA 510(k) clearance on 1987-12-11. The listed applicant is Laser Media. The 510(k) number is K872351.

When did FIBERLASE II ND:YAG LASER FOR PULMONARY USE receive FDA 510(k) clearance?

FIBERLASE II ND:YAG LASER FOR PULMONARY USE received FDA 510(k) clearance on 1987-12-11, under 510(k) number K872351.

Who is the listed applicant for FIBERLASE II ND:YAG LASER FOR PULMONARY USE?

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 FIBERLASE II ND:YAG LASER FOR PULMONARY USE?

The FDA product code for FIBERLASE II ND:YAG LASER FOR PULMONARY USE is LLO.

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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 MENORRHAGIAK872350FIBERLASE II ND:YAG LASER FOR GASTRO.&UROLOGY USEK872031UNI-FIBER NON-REPAIRABLE FIBER DELIVERY SYSTEMK863428SINGLE USE LASER FIBER DELIVERY SYSTEM FOR ND: YAGK863583CHANGE IN FIBERLASE 100 ND:YAG MEDICAL LASERK862444FIBERLASE 100 MEDICAL LASER SYS/ND:YAG MENORRHAGIA

View all 12 devices →

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.

K884815SLT CLMD CONTACT LASERSurgical Laser Technologies, Inc.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 USELaserguide

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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