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FDA 510(k)

STINGRAY BIPOLAR FORCEPS

K-Number: K123478 · 2013-05-10

ApplicantStingray Surgical Products
Decision Date2013-05-10
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STINGRAY BIPOLAR FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Stingray Surgical Products. It received FDA 510(k) clearance on 2013-05-10 under 510(k) number K123478. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STINGRAY BIPOLAR FORCEPS?

STINGRAY BIPOLAR FORCEPS is a medical device that received FDA 510(k) clearance on 2013-05-10. The listed applicant is Stingray Surgical Products. The 510(k) number is K123478.

When did STINGRAY BIPOLAR FORCEPS receive FDA 510(k) clearance?

STINGRAY BIPOLAR FORCEPS received FDA 510(k) clearance on 2013-05-10, under 510(k) number K123478.

Who is the listed applicant for STINGRAY BIPOLAR FORCEPS?

The FDA 510(k) record lists Stingray Surgical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STINGRAY BIPOLAR FORCEPS?

The FDA product code for STINGRAY BIPOLAR FORCEPS is GEI.

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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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