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 a medical device manufactured by Medline Industries, Inc.. It received FDA 510(k) clearance on 2022-11-18 under approval 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. It is manufactured by Medline Industries, Inc.. The 510(k) number is K212911.
When was Konig Mogen Clamp approved by the FDA?
Konig Mogen Clamp received FDA 510(k) clearance on 2022-11-18, under approval number K212911.
What company makes Konig Mogen Clamp?
Konig Mogen Clamp is manufactured by Medline Industries, Inc..
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.