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FDA 510(k)

CASTLE SERIES 100HC STEAM STERILIZERS

K-Number: K994314 · 2000-02-16

Decision Date2000-02-16
Product CodeFLE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CASTLE SERIES 100HC STEAM STERILIZERS 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 2000-02-16 under 510(k) number K994314. 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 SERIES 100HC STEAM STERILIZERS?

CASTLE SERIES 100HC STEAM STERILIZERS is a medical device that received FDA 510(k) clearance on 2000-02-16. The listed applicant is Getinge/Castle, Inc.. The 510(k) number is K994314.

When did CASTLE SERIES 100HC STEAM STERILIZERS receive FDA 510(k) clearance?

CASTLE SERIES 100HC STEAM STERILIZERS received FDA 510(k) clearance on 2000-02-16, under 510(k) number K994314.

Who is the listed applicant for CASTLE SERIES 100HC STEAM STERILIZERS?

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 SERIES 100HC STEAM STERILIZERS?

The FDA product code for CASTLE SERIES 100HC STEAM STERILIZERS 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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