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FDA 510(k)

WAGNER STERISET STERILIZATION CONTAINER

K-Number: K041096 · 2005-06-03

ApplicantWagner GmbH
Decision Date2005-06-03
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

WAGNER STERISET STERILIZATION CONTAINER is the device name listed in this FDA 510(k) record. The listed applicant is Wagner GmbH. It received FDA 510(k) clearance on 2005-06-03 under 510(k) number K041096. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WAGNER STERISET STERILIZATION CONTAINER?

WAGNER STERISET STERILIZATION CONTAINER is a medical device that received FDA 510(k) clearance on 2005-06-03. The listed applicant is Wagner GmbH. The 510(k) number is K041096.

When did WAGNER STERISET STERILIZATION CONTAINER receive FDA 510(k) clearance?

WAGNER STERISET STERILIZATION CONTAINER received FDA 510(k) clearance on 2005-06-03, under 510(k) number K041096.

Who is the listed applicant for WAGNER STERISET STERILIZATION CONTAINER?

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

What is the FDA product code for WAGNER STERISET STERILIZATION CONTAINER?

The FDA product code for WAGNER STERISET STERILIZATION CONTAINER is FRG.

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Related Devices (Code: FRG)

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

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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