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FDA 510(k)

C CHANGE SOLUTION WARMER

K-Number: K051819 · 2005-08-15

Decision Date2005-08-15
Product CodeLHC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

C CHANGE SOLUTION WARMER is the device name listed in this FDA 510(k) record. The listed applicant is C Change Surgical, LLC. It received FDA 510(k) clearance on 2005-08-15 under 510(k) number K051819. The device is classified under product code LHC. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the C CHANGE SOLUTION WARMER?

C CHANGE SOLUTION WARMER is a medical device that received FDA 510(k) clearance on 2005-08-15. The listed applicant is C Change Surgical, LLC. The 510(k) number is K051819.

When did C CHANGE SOLUTION WARMER receive FDA 510(k) clearance?

C CHANGE SOLUTION WARMER received FDA 510(k) clearance on 2005-08-15, under 510(k) number K051819.

Who is the listed applicant for C CHANGE SOLUTION WARMER?

The FDA 510(k) record lists C Change Surgical, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for C CHANGE SOLUTION WARMER?

The FDA product code for C CHANGE SOLUTION WARMER is LHC.

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 C Change Surgical, LLC 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: LHC)

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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