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FDA 510(k)

CeraPutty

K-Number: K232299 · 2023-09-29

ApplicantMeta Biomed Co., Ltd.
Decision Date2023-09-29
Product CodeKIF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CeraPutty is a medical device manufactured by Meta Biomed Co., Ltd.. It received FDA 510(k) clearance on 2023-09-29 under approval number K232299. The device is classified under product code KIF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CeraPutty?

CeraPutty is a medical device that received FDA 510(k) clearance on 2023-09-29. It is manufactured by Meta Biomed Co., Ltd.. The 510(k) number is K232299.

When was CeraPutty approved by the FDA?

CeraPutty received FDA 510(k) clearance on 2023-09-29, under approval number K232299.

What company makes CeraPutty?

CeraPutty is manufactured by Meta Biomed Co., Ltd..

What is the FDA product code for CeraPutty?

The FDA product code for CeraPutty is KIF.

Other Devices by Meta Biomed Co., Ltd.

K181689Nexcomp K180802Meta P&Bond K171449Metacem K190724MD-Temp Plus K190503CeraSeal K190510GuttaSil

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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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