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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 the device name listed in this FDA 510(k) record. The listed applicant is Carrtech Corp. It received FDA 510(k) clearance on 2025-04-18 under 510(k) 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. The listed applicant is Carrtech Corp. The 510(k) number is K240355.

When did FROG (Filter Removal of Glass) receive FDA 510(k) clearance?

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

Who is the listed applicant for FROG (Filter Removal of Glass)?

The FDA 510(k) record lists Carrtech Corp as the applicant. This does not by itself establish the device manufacturer.

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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Related Devices (Code: FMI)

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.

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Official Source

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