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FDA 510(k)

FROG (Filter Removal of Glass)

K-Number: K240355 · 2025-04-18

ApplicantCarrtech Corp
Decision Date2025-04-18
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FROG (Filter Removal of Glass) is a medical device manufactured by Carrtech Corp. It received FDA 510(k) clearance on 2025-04-18 under approval number K240355. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FROG (Filter Removal of Glass)?

FROG (Filter Removal of Glass) is a medical device that received FDA 510(k) clearance on 2025-04-18. It is manufactured by Carrtech Corp. The 510(k) number is K240355.

When was FROG (Filter Removal of Glass) approved by the FDA?

FROG (Filter Removal of Glass) received FDA 510(k) clearance on 2025-04-18, under approval number K240355.

What company makes FROG (Filter Removal of Glass)?

FROG (Filter Removal of Glass) is manufactured by Carrtech Corp.

What is the FDA product code for FROG (Filter Removal of Glass)?

The FDA product code for FROG (Filter Removal of Glass) is FMI.

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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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