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FDA 510(k)

MEDITRON MG-1000 MONOPOLAR GENERATOR

K-Number: K882049 · 1988-08-05

ApplicantXylog Corp.
Decision Date1988-08-05
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEDITRON MG-1000 MONOPOLAR GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Xylog Corp.. It received FDA 510(k) clearance on 1988-08-05 under 510(k) number K882049. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDITRON MG-1000 MONOPOLAR GENERATOR?

MEDITRON MG-1000 MONOPOLAR GENERATOR is a medical device that received FDA 510(k) clearance on 1988-08-05. The listed applicant is Xylog Corp.. The 510(k) number is K882049.

When did MEDITRON MG-1000 MONOPOLAR GENERATOR receive FDA 510(k) clearance?

MEDITRON MG-1000 MONOPOLAR GENERATOR received FDA 510(k) clearance on 1988-08-05, under 510(k) number K882049.

Who is the listed applicant for MEDITRON MG-1000 MONOPOLAR GENERATOR?

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 MG-1000 MONOPOLAR GENERATOR?

The FDA product code for MEDITRON MG-1000 MONOPOLAR GENERATOR is GEI.

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 SETK882048MEDITRON ENDOLAV MODEL EL-100K874798MEDITRON BI-2000 BIPOLAR GENERATOR W/IRRIGATION

Related Devices (Code: GEI)

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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