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FDA 510(k)

LASEGUIDE 600A, 600B, 400A, 400B FOR PULMONARY USE

K-Number: K880592 · 1988-04-25

ApplicantLaser Peripherals, LLC
Decision Date1988-04-25
Product CodeLLO
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

LASEGUIDE 600A, 600B, 400A, 400B FOR PULMONARY USE is the device name listed in this FDA 510(k) record. The listed applicant is Laser Peripherals, LLC. It received FDA 510(k) clearance on 1988-04-25 under 510(k) number K880592. 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 LASEGUIDE 600A, 600B, 400A, 400B FOR PULMONARY USE?

LASEGUIDE 600A, 600B, 400A, 400B FOR PULMONARY USE is a medical device that received FDA 510(k) clearance on 1988-04-25. The listed applicant is Laser Peripherals, LLC. The 510(k) number is K880592.

When did LASEGUIDE 600A, 600B, 400A, 400B FOR PULMONARY USE receive FDA 510(k) clearance?

LASEGUIDE 600A, 600B, 400A, 400B FOR PULMONARY USE received FDA 510(k) clearance on 1988-04-25, under 510(k) number K880592.

Who is the listed applicant for LASEGUIDE 600A, 600B, 400A, 400B FOR PULMONARY USE?

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

What is the FDA product code for LASEGUIDE 600A, 600B, 400A, 400B FOR PULMONARY USE?

The FDA product code for LASEGUIDE 600A, 600B, 400A, 400B FOR PULMONARY USE is LLO.

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Other records listing Laser Peripherals, LLC 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.

K170366Laser Peripherals, LLC Family of Bare Laser FibersK030959BARE LASER FIBER MODELS DBLF-40, DBLF-60, DBLF-60-1, DCLF-600B, DSLF-60, DBLF-100K011207LASER PERIPHERALS REUSABLE HOLMIUM FIBERK992083SCATTERFREE LATERAL EMITTING FIBERK974229LS-905 FIBERCHOICE ADAPTER SYSTEMK972272LASER PERIPHERALS HOLMIUM BARE FIBERS

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.K880170MODEL 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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