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)

ECLIPSE 2100(TM), MODIFICATION

K-Number: K924213 · 1993-07-13

ApplicantElipse Surgical Technologies, Inc.
Decision Date1993-07-13
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ECLIPSE 2100(TM), MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Elipse Surgical Technologies, Inc.. It received FDA 510(k) clearance on 1993-07-13 under 510(k) number K924213. 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 ECLIPSE 2100(TM), MODIFICATION?

ECLIPSE 2100(TM), MODIFICATION is a medical device that received FDA 510(k) clearance on 1993-07-13. The listed applicant is Elipse Surgical Technologies, Inc.. The 510(k) number is K924213.

When did ECLIPSE 2100(TM), MODIFICATION receive FDA 510(k) clearance?

ECLIPSE 2100(TM), MODIFICATION received FDA 510(k) clearance on 1993-07-13, under 510(k) number K924213.

Who is the listed applicant for ECLIPSE 2100(TM), MODIFICATION?

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

What is the FDA product code for ECLIPSE 2100(TM), MODIFICATION?

The FDA product code for ECLIPSE 2100(TM), MODIFICATION 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.

↑