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FDA 510(k)

OMNI-MATRIX

K-Number: K930151 · 1993-09-23

ApplicantInnovative Technology , Ltd.
Decision Date1993-09-23
Product CodeJEP
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

OMNI-MATRIX is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Technology , Ltd.. It received FDA 510(k) clearance on 1993-09-23 under 510(k) number K930151. The device is classified under product code JEP. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OMNI-MATRIX?

OMNI-MATRIX is a medical device that received FDA 510(k) clearance on 1993-09-23. The listed applicant is Innovative Technology , Ltd.. The 510(k) number is K930151.

When did OMNI-MATRIX receive FDA 510(k) clearance?

OMNI-MATRIX received FDA 510(k) clearance on 1993-09-23, under 510(k) number K930151.

Who is the listed applicant for OMNI-MATRIX?

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

What is the FDA product code for OMNI-MATRIX?

The FDA product code for OMNI-MATRIX is JEP.

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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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