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FDA 510(k)

CASTLE MODEL 233HC STEAM STERILIZER

K-Number: K003441 · 2001-01-02

Decision Date2001-01-02
Product CodeFLE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CASTLE MODEL 233HC STEAM STERILIZER is the device name listed in this FDA 510(k) record. The listed applicant is Getinge/Castle, Inc.. It received FDA 510(k) clearance on 2001-01-02 under 510(k) number K003441. The device is classified under product code FLE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CASTLE MODEL 233HC STEAM STERILIZER?

CASTLE MODEL 233HC STEAM STERILIZER is a medical device that received FDA 510(k) clearance on 2001-01-02. The listed applicant is Getinge/Castle, Inc.. The 510(k) number is K003441.

When did CASTLE MODEL 233HC STEAM STERILIZER receive FDA 510(k) clearance?

CASTLE MODEL 233HC STEAM STERILIZER received FDA 510(k) clearance on 2001-01-02, under 510(k) number K003441.

Who is the listed applicant for CASTLE MODEL 233HC STEAM STERILIZER?

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

What is the FDA product code for CASTLE MODEL 233HC STEAM STERILIZER?

The FDA product code for CASTLE MODEL 233HC STEAM STERILIZER is FLE.

Related Clinical Trials

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.

Other records listing Getinge/Castle, Inc. as applicant

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.

View all 9 devices →

Related Devices (Code: FLE)

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.

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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