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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 the device name listed in this FDA 510(k) record. The listed applicant is Fujifilm Medwork GmbH. It received FDA 510(k) clearance on 2022-06-01 under 510(k) 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. The listed applicant is Fujifilm Medwork GmbH. The 510(k) number is K221264.

When did FROG Forceps Valve (VAL1-F1-100) receive FDA 510(k) clearance?

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

Who is the listed applicant for FROG Forceps Valve (VAL1-F1-100)?

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

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 records listing Fujifilm Medwork GmbH as applicant

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.

Related Devices (Code: ODC)

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.

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.