FDA 510(k)

OLYMPUS STERILIZATION TRAYS

K-Number: K033222 · 2004-08-02

Decision Date2004-08-02

Product CodeKCT

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

OLYMPUS STERILIZATION TRAYS is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Winter & Ibe GmbH. It received FDA 510(k) clearance on 2004-08-02 under 510(k) number K033222. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OLYMPUS STERILIZATION TRAYS?

OLYMPUS STERILIZATION TRAYS is a medical device that received FDA 510(k) clearance on 2004-08-02. The listed applicant is Olympus Winter & Ibe GmbH. The 510(k) number is K033222.

When did OLYMPUS STERILIZATION TRAYS receive FDA 510(k) clearance?

OLYMPUS STERILIZATION TRAYS received FDA 510(k) clearance on 2004-08-02, under 510(k) number K033222.

Who is the listed applicant for OLYMPUS STERILIZATION TRAYS?

The FDA 510(k) record lists Olympus Winter & Ibe GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OLYMPUS STERILIZATION TRAYS?

The FDA product code for OLYMPUS STERILIZATION TRAYS is KCT.

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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.