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FDA 510(k)

DENE BRIDGE

K-Number: K903672 · 1990-12-05

ApplicantDirotian Pty. , Ltd.
Decision Date1990-12-05
Product CodeEKO
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENE BRIDGE is the device name listed in this FDA 510(k) record. The listed applicant is Dirotian Pty. , Ltd.. It received FDA 510(k) clearance on 1990-12-05 under 510(k) number K903672. The device is classified under product code EKO. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENE BRIDGE?

DENE BRIDGE is a medical device that received FDA 510(k) clearance on 1990-12-05. The listed applicant is Dirotian Pty. , Ltd.. The 510(k) number is K903672.

When did DENE BRIDGE receive FDA 510(k) clearance?

DENE BRIDGE received FDA 510(k) clearance on 1990-12-05, under 510(k) number K903672.

Who is the listed applicant for DENE BRIDGE?

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

What is the FDA product code for DENE BRIDGE?

The FDA product code for DENE BRIDGE is EKO.

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Related Devices (Code: EKO)

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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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