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FDA 510(k)

MICRO-FRANCE ELECTROSURGICAL INSTRUMENTS, VARIOUS

K-Number: K993655 · 1999-12-21

ApplicantXomed, Inc.
Decision Date1999-12-21
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MICRO-FRANCE ELECTROSURGICAL INSTRUMENTS, VARIOUS is the device name listed in this FDA 510(k) record. The listed applicant is Xomed, Inc.. It received FDA 510(k) clearance on 1999-12-21 under 510(k) number K993655. 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 MICRO-FRANCE ELECTROSURGICAL INSTRUMENTS, VARIOUS?

MICRO-FRANCE ELECTROSURGICAL INSTRUMENTS, VARIOUS is a medical device that received FDA 510(k) clearance on 1999-12-21. The listed applicant is Xomed, Inc.. The 510(k) number is K993655.

When did MICRO-FRANCE ELECTROSURGICAL INSTRUMENTS, VARIOUS receive FDA 510(k) clearance?

MICRO-FRANCE ELECTROSURGICAL INSTRUMENTS, VARIOUS received FDA 510(k) clearance on 1999-12-21, under 510(k) number K993655.

Who is the listed applicant for MICRO-FRANCE ELECTROSURGICAL INSTRUMENTS, VARIOUS?

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

What is the FDA product code for MICRO-FRANCE ELECTROSURGICAL INSTRUMENTS, VARIOUS?

The FDA product code for MICRO-FRANCE ELECTROSURGICAL INSTRUMENTS, VARIOUS 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.

Other records listing Xomed, Inc. 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.

View all 82 devices →

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.

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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