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FDA 510(k)

MEDITRON BI-2000 BIPOLAR GENERATOR W/IRRIGATION

K-Number: K874798 · 1988-02-24

ApplicantXylog Corp.
Decision Date1988-02-24
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEDITRON BI-2000 BIPOLAR GENERATOR W/IRRIGATION is the device name listed in this FDA 510(k) record. The listed applicant is Xylog Corp.. It received FDA 510(k) clearance on 1988-02-24 under 510(k) number K874798. 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 BI-2000 BIPOLAR GENERATOR W/IRRIGATION?

MEDITRON BI-2000 BIPOLAR GENERATOR W/IRRIGATION is a medical device that received FDA 510(k) clearance on 1988-02-24. The listed applicant is Xylog Corp.. The 510(k) number is K874798.

When did MEDITRON BI-2000 BIPOLAR GENERATOR W/IRRIGATION receive FDA 510(k) clearance?

MEDITRON BI-2000 BIPOLAR GENERATOR W/IRRIGATION received FDA 510(k) clearance on 1988-02-24, under 510(k) number K874798.

Who is the listed applicant for MEDITRON BI-2000 BIPOLAR GENERATOR W/IRRIGATION?

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 BI-2000 BIPOLAR GENERATOR W/IRRIGATION?

The FDA product code for MEDITRON BI-2000 BIPOLAR GENERATOR W/IRRIGATION is GEI.

Related Clinical Trials

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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-100K882049MEDITRON MG-1000 MONOPOLAR GENERATOR

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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