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FDA 510(k)

CONSOLIDATED SR AND SSE MC-SERIES STEAM STERILIZER

K-Number: K041833 · 2004-12-10

Decision Date2004-12-10
Product CodeFLE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CONSOLIDATED SR AND SSE MC-SERIES STEAM STERILIZER is the device name listed in this FDA 510(k) record. The listed applicant is Consolidated Machine Corp.. It received FDA 510(k) clearance on 2004-12-10 under 510(k) number K041833. 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 CONSOLIDATED SR AND SSE MC-SERIES STEAM STERILIZER?

CONSOLIDATED SR AND SSE MC-SERIES STEAM STERILIZER is a medical device that received FDA 510(k) clearance on 2004-12-10. The listed applicant is Consolidated Machine Corp.. The 510(k) number is K041833.

When did CONSOLIDATED SR AND SSE MC-SERIES STEAM STERILIZER receive FDA 510(k) clearance?

CONSOLIDATED SR AND SSE MC-SERIES STEAM STERILIZER received FDA 510(k) clearance on 2004-12-10, under 510(k) number K041833.

Who is the listed applicant for CONSOLIDATED SR AND SSE MC-SERIES STEAM STERILIZER?

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

What is the FDA product code for CONSOLIDATED SR AND SSE MC-SERIES STEAM STERILIZER?

The FDA product code for CONSOLIDATED SR AND SSE MC-SERIES 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 Consolidated Machine Corp. 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.

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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