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FDA 510(k)

STIMULUS/DISSECTION INSTRUMENTS, BALL-TIP PROBES

K-Number: K031003 · 2003-04-11

ApplicantMedtronic Xomed, Inc.
Decision Date2003-04-11
Product CodeETN
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

STIMULUS/DISSECTION INSTRUMENTS, BALL-TIP PROBES is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Xomed, Inc.. It received FDA 510(k) clearance on 2003-04-11 under 510(k) number K031003. The device is classified under product code ETN. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STIMULUS/DISSECTION INSTRUMENTS, BALL-TIP PROBES?

STIMULUS/DISSECTION INSTRUMENTS, BALL-TIP PROBES is a medical device that received FDA 510(k) clearance on 2003-04-11. The listed applicant is Medtronic Xomed, Inc.. The 510(k) number is K031003.

When did STIMULUS/DISSECTION INSTRUMENTS, BALL-TIP PROBES receive FDA 510(k) clearance?

STIMULUS/DISSECTION INSTRUMENTS, BALL-TIP PROBES received FDA 510(k) clearance on 2003-04-11, under 510(k) number K031003.

Who is the listed applicant for STIMULUS/DISSECTION INSTRUMENTS, BALL-TIP PROBES?

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

What is the FDA product code for STIMULUS/DISSECTION INSTRUMENTS, BALL-TIP PROBES?

The FDA product code for STIMULUS/DISSECTION INSTRUMENTS, BALL-TIP PROBES is ETN.

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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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