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FDA 510(k)

LASEGUIDE 600A, 600B, 400A, 400B FOR OB-GYN USE

K-Number: K880591 · 1988-06-01

ApplicantLaser Peripherals, LLC
Decision Date1988-06-01
Product CodeHHR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LASEGUIDE 600A, 600B, 400A, 400B FOR OB-GYN 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 1988-06-01 under 510(k) number K880591. The device is classified under product code HHR. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LASEGUIDE 600A, 600B, 400A, 400B FOR OB-GYN USE?

LASEGUIDE 600A, 600B, 400A, 400B FOR OB-GYN USE is a medical device that received FDA 510(k) clearance on 1988-06-01. The listed applicant is Laser Peripherals, LLC. The 510(k) number is K880591.

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

LASEGUIDE 600A, 600B, 400A, 400B FOR OB-GYN USE received FDA 510(k) clearance on 1988-06-01, under 510(k) number K880591.

Who is the listed applicant for LASEGUIDE 600A, 600B, 400A, 400B FOR OB-GYN 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 OB-GYN USE?

The FDA product code for LASEGUIDE 600A, 600B, 400A, 400B FOR OB-GYN USE is HHR.

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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

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Related Devices (Code: HHR)

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.

K881507ENDOCOAGULATOR MODEL 20 LASER & ACCESSORIESHgm Medical Laser Systems, Inc.K871875MODEL 5050 SURGILASER FOR OB-GYN USELasermatic, Inc.K875314GL-35 COLPOSCOPIC LASER SYSTEMLaser Engineering, Inc.K874615LASER CANNISTER FILTERMedical Marketing, Inc.K880930MDLS 4000,4900,6000,8000,8900 ND:YAG/1700 C02 LASECopper Lasersonics, Inc.K880991LASER OPTICAL CATHETER SYSTEMMedline Industries, 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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