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FDA 510(k)

CABLE, TRANSDUCER, MODEL 2400GN

K-Number: K083448 · 2009-08-20

ApplicantConmed Corporation
Decision Date2009-08-20
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CABLE, TRANSDUCER, MODEL 2400GN is the device name listed in this FDA 510(k) record. The listed applicant is Conmed Corporation. It received FDA 510(k) clearance on 2009-08-20 under 510(k) number K083448. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CABLE, TRANSDUCER, MODEL 2400GN?

CABLE, TRANSDUCER, MODEL 2400GN is a medical device that received FDA 510(k) clearance on 2009-08-20. The listed applicant is Conmed Corporation. The 510(k) number is K083448.

When did CABLE, TRANSDUCER, MODEL 2400GN receive FDA 510(k) clearance?

CABLE, TRANSDUCER, MODEL 2400GN received FDA 510(k) clearance on 2009-08-20, under 510(k) number K083448.

Who is the listed applicant for CABLE, TRANSDUCER, MODEL 2400GN?

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

What is the FDA product code for CABLE, TRANSDUCER, MODEL 2400GN?

The FDA product code for CABLE, TRANSDUCER, MODEL 2400GN is DQA.

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Related Devices (Code: DQA)

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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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