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FDA 510(k)

LASEGUIDE 600A, 600B, 400A, AND 400B

K-Number: K874680 · 1988-03-23

ApplicantLaser Peripherals, LLC
Decision Date1988-03-23
Product CodeFCS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LASEGUIDE 600A, 600B, 400A, AND 400B 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 1988-03-23 under 510(k) number K874680. The device is classified under product code FCS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LASEGUIDE 600A, 600B, 400A, AND 400B?

LASEGUIDE 600A, 600B, 400A, AND 400B is a medical device that received FDA 510(k) clearance on 1988-03-23. The listed applicant is Laser Peripherals, LLC. The 510(k) number is K874680.

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

LASEGUIDE 600A, 600B, 400A, AND 400B received FDA 510(k) clearance on 1988-03-23, under 510(k) number K874680.

Who is the listed applicant for LASEGUIDE 600A, 600B, 400A, AND 400B?

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, AND 400B?

The FDA product code for LASEGUIDE 600A, 600B, 400A, AND 400B is FCS.

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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: FCS)

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.

K061548STRYKER URETERAL ILLUMINATION SYSTEM IVStryker Corp.K982542STRYKER URETERAL ILLUMINATOR SYSTEM IIIStryker EndoscopyK943801URIGLOW TRANSILLUMINATING URETERIC STENT MODELRocket of London, Ltd.K945088GABRIEL URETERAL ILLUMINATOR SYSTEM IIGabriel Medical, Inc.K941506URETERAL ILLUMINATORApple Medical Corp.K940019GABRIEL URETERAL ILLUMINATOR SYSTEMGabriel Medical, 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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