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FDA 510(k)

Konig Mogen Clamp

K-Number: K212911 · 2022-11-18

ApplicantMedline Industries, Inc.
Decision Date2022-11-18
Product CodeHFX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Konig Mogen Clamp is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 2022-11-18 under 510(k) number K212911. The device is classified under product code HFX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Konig Mogen Clamp?

Konig Mogen Clamp is a medical device that received FDA 510(k) clearance on 2022-11-18. The listed applicant is Medline Industries, Inc.. The 510(k) number is K212911.

When did Konig Mogen Clamp receive FDA 510(k) clearance?

Konig Mogen Clamp received FDA 510(k) clearance on 2022-11-18, under 510(k) number K212911.

Who is the listed applicant for Konig Mogen Clamp?

The FDA 510(k) record lists Medline Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Konig Mogen Clamp?

The FDA product code for Konig Mogen Clamp is HFX.

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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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