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FDA 510(k)

FROG Forceps Valve (VAL1-F1-100)

K-Number: K221264 · 2022-06-01

Decision Date2022-06-01
Product CodeODC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FROG Forceps Valve (VAL1-F1-100) is a medical device manufactured by Fujifilm Medwork GmbH. It received FDA 510(k) clearance on 2022-06-01 under approval number K221264. The device is classified under product code ODC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FROG Forceps Valve (VAL1-F1-100)?

FROG Forceps Valve (VAL1-F1-100) is a medical device that received FDA 510(k) clearance on 2022-06-01. It is manufactured by Fujifilm Medwork GmbH. The 510(k) number is K221264.

When was FROG Forceps Valve (VAL1-F1-100) approved by the FDA?

FROG Forceps Valve (VAL1-F1-100) received FDA 510(k) clearance on 2022-06-01, under approval number K221264.

What company makes FROG Forceps Valve (VAL1-F1-100)?

FROG Forceps Valve (VAL1-F1-100) is manufactured by Fujifilm Medwork GmbH.

What is the FDA product code for FROG Forceps Valve (VAL1-F1-100)?

The FDA product code for FROG Forceps Valve (VAL1-F1-100) is ODC.

Other Devices by Fujifilm Medwork GmbH

Related Devices (Code: ODC)

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.