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FDA 510(k)

EM PROBE, EM PAD

K-Number: K024361 · 2003-10-09

ApplicantEm Probe, Inc.
Decision Date2003-10-09
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

EM PROBE, EM PAD is the device name listed in this FDA 510(k) record. The listed applicant is Em Probe, Inc.. It received FDA 510(k) clearance on 2003-10-09 under 510(k) number K024361. The device is classified under product code ILY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EM PROBE, EM PAD?

EM PROBE, EM PAD is a medical device that received FDA 510(k) clearance on 2003-10-09. The listed applicant is Em Probe, Inc.. The 510(k) number is K024361.

When did EM PROBE, EM PAD receive FDA 510(k) clearance?

EM PROBE, EM PAD received FDA 510(k) clearance on 2003-10-09, under 510(k) number K024361.

Who is the listed applicant for EM PROBE, EM PAD?

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

What is the FDA product code for EM PROBE, EM PAD?

The FDA product code for EM PROBE, EM PAD is ILY.

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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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