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FDA 510(k)

CARPL (CARPL)

K-Number: K232891 · 2024-03-27

ApplicantCarpl Ai, Inc.
Decision Date2024-03-27
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CARPL (CARPL) is a medical device manufactured by Carpl Ai, Inc.. It received FDA 510(k) clearance on 2024-03-27 under approval number K232891. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARPL (CARPL)?

CARPL (CARPL) is a medical device that received FDA 510(k) clearance on 2024-03-27. It is manufactured by Carpl Ai, Inc.. The 510(k) number is K232891.

When was CARPL (CARPL) approved by the FDA?

CARPL (CARPL) received FDA 510(k) clearance on 2024-03-27, under approval number K232891.

What company makes CARPL (CARPL)?

CARPL (CARPL) is manufactured by Carpl Ai, Inc..

What is the FDA product code for CARPL (CARPL)?

The FDA product code for CARPL (CARPL) is LLZ.

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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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