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FDA 510(k)

MICRO-MAX, MODEL 319

K-Number: K002404 · 2000-08-30

ApplicantTek Marketing, Inc.
Decision Date2000-08-30
Product CodeIXW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MICRO-MAX, MODEL 319 is the device name listed in this FDA 510(k) record. The listed applicant is Tek Marketing, Inc.. It received FDA 510(k) clearance on 2000-08-30 under 510(k) number K002404. The device is classified under product code IXW. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO-MAX, MODEL 319?

MICRO-MAX, MODEL 319 is a medical device that received FDA 510(k) clearance on 2000-08-30. The listed applicant is Tek Marketing, Inc.. The 510(k) number is K002404.

When did MICRO-MAX, MODEL 319 receive FDA 510(k) clearance?

MICRO-MAX, MODEL 319 received FDA 510(k) clearance on 2000-08-30, under 510(k) number K002404.

Who is the listed applicant for MICRO-MAX, MODEL 319?

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

What is the FDA product code for MICRO-MAX, MODEL 319?

The FDA product code for MICRO-MAX, MODEL 319 is IXW.

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Related Devices (Code: IXW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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