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)

FEMTEC LASER MICROKERATOME

K-Number: K033354 · 2004-02-18

Applicant20/10 Perfect Vision Optische Gerate GmbH
Decision Date2004-02-18
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FEMTEC LASER MICROKERATOME is the device name listed in this FDA 510(k) record. The listed applicant is 20/10 Perfect Vision Optische Gerate GmbH. It received FDA 510(k) clearance on 2004-02-18 under 510(k) number K033354. 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 FEMTEC LASER MICROKERATOME?

FEMTEC LASER MICROKERATOME is a medical device that received FDA 510(k) clearance on 2004-02-18. The listed applicant is 20/10 Perfect Vision Optische Gerate GmbH. The 510(k) number is K033354.

When did FEMTEC LASER MICROKERATOME receive FDA 510(k) clearance?

FEMTEC LASER MICROKERATOME received FDA 510(k) clearance on 2004-02-18, under 510(k) number K033354.

Who is the listed applicant for FEMTEC LASER MICROKERATOME?

The FDA 510(k) record lists 20/10 Perfect Vision Optische Gerate GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FEMTEC LASER MICROKERATOME?

The FDA product code for FEMTEC LASER MICROKERATOME 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

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.

↑