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FDA 510(k)

MODEL 733HC GRAVITY/VACUUM STEAM STERILIZER

K-Number: K020590 · 2002-03-20

Decision Date2002-03-20
Product CodeFLE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODEL 733HC GRAVITY/VACUUM 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 2002-03-20 under 510(k) number K020590. 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 MODEL 733HC GRAVITY/VACUUM STEAM STERILIZER?

MODEL 733HC GRAVITY/VACUUM STEAM STERILIZER is a medical device that received FDA 510(k) clearance on 2002-03-20. The listed applicant is Getinge/Castle, Inc.. The 510(k) number is K020590.

When did MODEL 733HC GRAVITY/VACUUM STEAM STERILIZER receive FDA 510(k) clearance?

MODEL 733HC GRAVITY/VACUUM STEAM STERILIZER received FDA 510(k) clearance on 2002-03-20, under 510(k) number K020590.

Who is the listed applicant for MODEL 733HC GRAVITY/VACUUM 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 MODEL 733HC GRAVITY/VACUUM STEAM STERILIZER?

The FDA product code for MODEL 733HC GRAVITY/VACUUM 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

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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