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FDA 510(k)

MODEL 5050 SURGILASER FOR OB-GYN USE

K-Number: K871875 · 1988-08-22

ApplicantLasermatic, Inc.
Decision Date1988-08-22
Product CodeHHR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MODEL 5050 SURGILASER FOR OB-GYN USE is the device name listed in this FDA 510(k) record. The listed applicant is Lasermatic, Inc.. It received FDA 510(k) clearance on 1988-08-22 under 510(k) number K871875. 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 MODEL 5050 SURGILASER FOR OB-GYN USE?

MODEL 5050 SURGILASER FOR OB-GYN USE is a medical device that received FDA 510(k) clearance on 1988-08-22. The listed applicant is Lasermatic, Inc.. The 510(k) number is K871875.

When did MODEL 5050 SURGILASER FOR OB-GYN USE receive FDA 510(k) clearance?

MODEL 5050 SURGILASER FOR OB-GYN USE received FDA 510(k) clearance on 1988-08-22, under 510(k) number K871875.

Who is the listed applicant for MODEL 5050 SURGILASER FOR OB-GYN USE?

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

What is the FDA product code for MODEL 5050 SURGILASER FOR OB-GYN USE?

The FDA product code for MODEL 5050 SURGILASER FOR OB-GYN USE is HHR.

Related Clinical Trials

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Other records listing Lasermatic, Inc. 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.

K903131LASERMATIC SUPERCOMBO(TM) SURGICAL LASER SYSTEMK901638MODIFIED COMBOLASER 5050 & NEW MODEL 5050 VER. 33K893529COMBOLASER MODEL 5050K871934MODEL 5050 SURGILASER FOR GASTRO-INTESTINAL USEK871932MODEL 5050 SURGILASER FOR UROLOGY USEK871933MODEL 5050 SURGILASER FOR NEUROSURGERY USE

View all 8 devices →

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.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.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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