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FDA 510(k)

KTP/532 LASER FOR OB-GYN USE

K-Number: K874837 · 1988-03-14

ApplicantLaserscope
Decision Date1988-03-14
Product CodeHHR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

KTP/532 LASER FOR OB-GYN USE is the device name listed in this FDA 510(k) record. The listed applicant is Laserscope. It received FDA 510(k) clearance on 1988-03-14 under 510(k) number K874837. 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 KTP/532 LASER FOR OB-GYN USE?

KTP/532 LASER FOR OB-GYN USE is a medical device that received FDA 510(k) clearance on 1988-03-14. The listed applicant is Laserscope. The 510(k) number is K874837.

When did KTP/532 LASER FOR OB-GYN USE receive FDA 510(k) clearance?

KTP/532 LASER FOR OB-GYN USE received FDA 510(k) clearance on 1988-03-14, under 510(k) number K874837.

Who is the listed applicant for KTP/532 LASER FOR OB-GYN USE?

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

What is the FDA product code for KTP/532 LASER FOR OB-GYN USE?

The FDA product code for KTP/532 LASER FOR OB-GYN USE is HHR.

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Other records listing Laserscope 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.

K062719GREENLIGHT HPS SERIES SURGICAL LASER SYSTEM & ACCESSORIESK061646LASERSCOPE GUIDED DELIVERY DEVICE (GDD) CYSTOURETHROSCOPE & ACCESSORIESK034011GEMINI SURGICAL LASER SYSTEM & ACCESSORIESK024206AURA ISURGICAL LASER SYSTEM & ACCESSORIESK020021LYRA SURGICAL LASER SYSTEM AND ACCESSIORIES (ND:YAG CONFIGURATION)K010834LYRA SERIES SURGICAL LASER SYSTEM & ACCESSORIES

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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.K880591LASEGUIDE 600A, 600B, 400A, 400B FOR OB-GYN USELaser Peripherals, LLCK880930MDLS 4000,4900,6000,8000,8900 ND:YAG/1700 C02 LASECopper Lasersonics, 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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