FDA 510(k)

CHRISTOUDIAS SLIM TIP ELECTRODE INSERT

K-Number: K992345 · 1999-09-10

Decision Date1999-09-10

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

CHRISTOUDIAS SLIM TIP ELECTRODE INSERT is the device name listed in this FDA 510(k) record. The listed applicant is Innervision, Inc.. It received FDA 510(k) clearance on 1999-09-10 under 510(k) number K992345. 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 CHRISTOUDIAS SLIM TIP ELECTRODE INSERT?

CHRISTOUDIAS SLIM TIP ELECTRODE INSERT is a medical device that received FDA 510(k) clearance on 1999-09-10. The listed applicant is Innervision, Inc.. The 510(k) number is K992345.

When did CHRISTOUDIAS SLIM TIP ELECTRODE INSERT receive FDA 510(k) clearance?

CHRISTOUDIAS SLIM TIP ELECTRODE INSERT received FDA 510(k) clearance on 1999-09-10, under 510(k) number K992345.

Who is the listed applicant for CHRISTOUDIAS SLIM TIP ELECTRODE INSERT?

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

What is the FDA product code for CHRISTOUDIAS SLIM TIP ELECTRODE INSERT?

The FDA product code for CHRISTOUDIAS SLIM TIP ELECTRODE INSERT is GEI.

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Other records listing Innervision, Inc. as applicant

K991877MACMED PAEDIATRIC INTRAMEDULLARY NAIL K982428CHRISTOUDIAS GAUZE DISSECTOR (LAPAROSCOPIC HAND INSTRUMENT)K940731INNERVISION INC. CANNULA/TROCAR,MULTIPLE TYPES K940750INNERVISION,INC. LAPAROSCOPIC ELECTRODES K940718INNERVISION INC. LAPAROSCOPIC HAND INSTRUMENTS

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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.