Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CO2 LASER SYSTEMS & ARTHROGUIDE CO2 LASER FIBER

K-Number: K893832 · 1989-08-09

ApplicantHeraeus Lasersonics, Inc.
Decision Date1989-08-09
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CO2 LASER SYSTEMS & ARTHROGUIDE CO2 LASER FIBER is the device name listed in this FDA 510(k) record. The listed applicant is Heraeus Lasersonics, Inc.. It received FDA 510(k) clearance on 1989-08-09 under 510(k) number K893832. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CO2 LASER SYSTEMS & ARTHROGUIDE CO2 LASER FIBER?

CO2 LASER SYSTEMS & ARTHROGUIDE CO2 LASER FIBER is a medical device that received FDA 510(k) clearance on 1989-08-09. The listed applicant is Heraeus Lasersonics, Inc.. The 510(k) number is K893832.

When did CO2 LASER SYSTEMS & ARTHROGUIDE CO2 LASER FIBER receive FDA 510(k) clearance?

CO2 LASER SYSTEMS & ARTHROGUIDE CO2 LASER FIBER received FDA 510(k) clearance on 1989-08-09, under 510(k) number K893832.

Who is the listed applicant for CO2 LASER SYSTEMS & ARTHROGUIDE CO2 LASER FIBER?

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

What is the FDA product code for CO2 LASER SYSTEMS & ARTHROGUIDE CO2 LASER FIBER?

The FDA product code for CO2 LASER SYSTEMS & ARTHROGUIDE CO2 LASER FIBER is GEX. This falls under the Gastroenterology category.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Heraeus Lasersonics, 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.

K933245ULTRALINE II STERILE DISPOSABLE FIBERK923896HERCULES MODEL 5060 AND 5100 ND:YAG LASER SYSTEMSK921807ULTRALINE STERILE DISPOSABLE FIBERK915578ND;YAG SURGICAL LASER SYSTEMSK915583CO2 LASER AND WAVEGUIDE DELIVERY SYSTEMS FOR THOR.K912618LASER SYSTEMS FOR PERCUTANEOUS LUMBAR DISCECTOMY

View all 38 devices →

Related Devices (Code: GEX)

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.

K254199PicoreMax (PicoreMax)BLUECORE COMPANY Co., Ltd.K252723Dynamis Pro FamilyFotona D.O.O.K241973SmartIPL_NI SystemLumenis Be, Ltd.K261047Dental Diode Laser Device (Laser-Pen)Guilin Kevin Peter Technology Co., Ltd.K261817Diode Laser Therapy System (PZ-BDT67-01, PZ-BDT67-02)Zhengzhou PZ Laser Slim Technology Co., Ltd.K261673LED Therapy Device (QLXY-01)Beijing Nubway S&T Co., Ltd.

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.

↑