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FDA 510(k)

CONTACT ND:YAG LASER FOR TREATMENT OF MENORRHAGIA

K-Number: K872253 · 1987-10-06

ApplicantSurgical Laser Technologies, Inc.
Decision Date1987-10-06
Product CodeHHR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CONTACT ND:YAG LASER FOR TREATMENT OF MENORRHAGIA is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Laser Technologies, Inc.. It received FDA 510(k) clearance on 1987-10-06 under 510(k) number K872253. 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 CONTACT ND:YAG LASER FOR TREATMENT OF MENORRHAGIA?

CONTACT ND:YAG LASER FOR TREATMENT OF MENORRHAGIA is a medical device that received FDA 510(k) clearance on 1987-10-06. The listed applicant is Surgical Laser Technologies, Inc.. The 510(k) number is K872253.

When did CONTACT ND:YAG LASER FOR TREATMENT OF MENORRHAGIA receive FDA 510(k) clearance?

CONTACT ND:YAG LASER FOR TREATMENT OF MENORRHAGIA received FDA 510(k) clearance on 1987-10-06, under 510(k) number K872253.

Who is the listed applicant for CONTACT ND:YAG LASER FOR TREATMENT OF MENORRHAGIA?

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

What is the FDA product code for CONTACT ND:YAG LASER FOR TREATMENT OF MENORRHAGIA?

The FDA product code for CONTACT ND:YAG LASER FOR TREATMENT OF MENORRHAGIA is HHR.

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Other records listing Surgical Laser Technologies, 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.

K042211MODIFICATION TO: LASERPRO 810, 940, AND 980 DIODE DIODE LASER SYSTEMSK023624SLT VENOUS FIBER DELIVERY SYSTEMS, MODEL: 0041-6772/0041-6781/0041-6752/0041-6761/0041-6912/0041-6921K011409SLT LASERPRO CTH HOLMIUM LASER SYSTEMK010041SLT DIFFUSER FIBERK984018HEMOSLEEVE, MODEL 4.0MM, 5.5MMK983050PNEUMATIC CUTTER SYSTEM

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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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