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FDA 510(k)

E-STRIP

K-Number: K031769 · 2003-10-14

ApplicantEemso, Inc.
Decision Date2003-10-14
Product CodeEGJ
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

E-STRIP is the device name listed in this FDA 510(k) record. The listed applicant is Eemso, Inc.. It received FDA 510(k) clearance on 2003-10-14 under 510(k) number K031769. The device is classified under product code EGJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the E-STRIP?

E-STRIP is a medical device that received FDA 510(k) clearance on 2003-10-14. The listed applicant is Eemso, Inc.. The 510(k) number is K031769.

When did E-STRIP receive FDA 510(k) clearance?

E-STRIP received FDA 510(k) clearance on 2003-10-14, under 510(k) number K031769.

Who is the listed applicant for E-STRIP?

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

What is the FDA product code for E-STRIP?

The FDA product code for E-STRIP is EGJ.

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Related Devices (Code: EGJ)

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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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