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FDA 510(k)

MEDITRON ENDOLAV MODEL EL-100

K-Number: K882048 · 1988-10-31

ApplicantXylog Corp.
Decision Date1988-10-31
Product CodeKNS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MEDITRON ENDOLAV MODEL EL-100 is the device name listed in this FDA 510(k) record. The listed applicant is Xylog Corp.. It received FDA 510(k) clearance on 1988-10-31 under 510(k) number K882048. The device is classified under product code KNS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDITRON ENDOLAV MODEL EL-100?

MEDITRON ENDOLAV MODEL EL-100 is a medical device that received FDA 510(k) clearance on 1988-10-31. The listed applicant is Xylog Corp.. The 510(k) number is K882048.

When did MEDITRON ENDOLAV MODEL EL-100 receive FDA 510(k) clearance?

MEDITRON ENDOLAV MODEL EL-100 received FDA 510(k) clearance on 1988-10-31, under 510(k) number K882048.

Who is the listed applicant for MEDITRON ENDOLAV MODEL EL-100?

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

What is the FDA product code for MEDITRON ENDOLAV MODEL EL-100?

The FDA product code for MEDITRON ENDOLAV MODEL EL-100 is KNS.

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 Xylog Corp. 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.

K945970INSUFFLATOR FILTER TUBING SETK882049MEDITRON MG-1000 MONOPOLAR GENERATORK874798MEDITRON BI-2000 BIPOLAR GENERATOR W/IRRIGATION

Related Devices (Code: KNS)

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.

K262460Rezum SystemBoston ScientificK260962SphincterotomeTaewoong Medical Co., Ltd.K252388Vanquish Water Vapor Ablation DeviceFrancis Medical, Inc.K252889Single Use 3-Lumen Needle Knife V (KD-V441M, KD-V451M)Olympus Medical Systems CorporationK250945Single Use Preloaded Sphincterotome V (Distal Wire Guided) (KD-VC600 Series); Single Use Sphincterotome V (Distal Wire Guided) (KD-VC400 Series); Single Use 3-Lumen Sphincterotome (KD-V Series); Disposable Triple Lumen Sphincterotome (KD Series)Olympus Medical Systems Corp.K250351Single Use Electrosurgical Knife (KD-612L, KD-612U); Single Use Electrosurgical Knife (KD-620UR); Single Use Electrosurgical Knife (KD-650L, KD-650U)Olympus Medical Systems Corporation

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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