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FDA 510(k)

Carecube Negative Pressure Isolation Chamber

K-Number: K231256 · 2024-01-03

ApplicantCarecubes, Inc.
Decision Date2024-01-03
Product CodeLGM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Carecube Negative Pressure Isolation Chamber is a medical device manufactured by Carecubes, Inc.. It received FDA 510(k) clearance on 2024-01-03 under approval number K231256. The device is classified under product code LGM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Carecube Negative Pressure Isolation Chamber?

Carecube Negative Pressure Isolation Chamber is a medical device that received FDA 510(k) clearance on 2024-01-03. It is manufactured by Carecubes, Inc.. The 510(k) number is K231256.

When was Carecube Negative Pressure Isolation Chamber approved by the FDA?

Carecube Negative Pressure Isolation Chamber received FDA 510(k) clearance on 2024-01-03, under approval number K231256.

What company makes Carecube Negative Pressure Isolation Chamber?

Carecube Negative Pressure Isolation Chamber is manufactured by Carecubes, Inc..

What is the FDA product code for Carecube Negative Pressure Isolation Chamber?

The FDA product code for Carecube Negative Pressure Isolation Chamber is LGM.

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Official Source

View on FDA Database →

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