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FDA 510(k)

Boehringer Laboratories Liver Retractor

K-Number: K243399 · 2025-07-02

ApplicantBoehringer Laboratories, LLC
Decision Date2025-07-02
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Boehringer Laboratories Liver Retractor is the device name listed in this FDA 510(k) record. The listed applicant is Boehringer Laboratories, LLC. It received FDA 510(k) clearance on 2025-07-02 under 510(k) number K243399. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Boehringer Laboratories Liver Retractor?

Boehringer Laboratories Liver Retractor is a medical device that received FDA 510(k) clearance on 2025-07-02. The listed applicant is Boehringer Laboratories, LLC. The 510(k) number is K243399.

When did Boehringer Laboratories Liver Retractor receive FDA 510(k) clearance?

Boehringer Laboratories Liver Retractor received FDA 510(k) clearance on 2025-07-02, under 510(k) number K243399.

Who is the listed applicant for Boehringer Laboratories Liver Retractor?

The FDA 510(k) record lists Boehringer Laboratories, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Boehringer Laboratories Liver Retractor?

The FDA product code for Boehringer Laboratories Liver Retractor is GCJ.

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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.

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