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FDA 510(k)

SPARTAN MTS

K-Number: K002521 · 2000-11-13

ApplicantSpartan Marketing Group
Decision Date2000-11-13
Product CodeELC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SPARTAN MTS is the device name listed in this FDA 510(k) record. The listed applicant is Spartan Marketing Group. It received FDA 510(k) clearance on 2000-11-13 under 510(k) number K002521. The device is classified under product code ELC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPARTAN MTS?

SPARTAN MTS is a medical device that received FDA 510(k) clearance on 2000-11-13. The listed applicant is Spartan Marketing Group. The 510(k) number is K002521.

When did SPARTAN MTS receive FDA 510(k) clearance?

SPARTAN MTS received FDA 510(k) clearance on 2000-11-13, under 510(k) number K002521.

Who is the listed applicant for SPARTAN MTS?

The FDA 510(k) record lists Spartan Marketing Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPARTAN MTS?

The FDA product code for SPARTAN MTS is ELC.

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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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