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FDA 510(k)

1-CCD ENDOCAM 5520 SYSTEM

K-Number: K023659 · 2003-01-29

ApplicantRichard Wolf Medical Instruments Corp.
Decision Date2003-01-29
Product CodeFET
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

1-CCD ENDOCAM 5520 SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corp.. It received FDA 510(k) clearance on 2003-01-29 under 510(k) number K023659. The device is classified under product code FET. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 1-CCD ENDOCAM 5520 SYSTEM?

1-CCD ENDOCAM 5520 SYSTEM is a medical device that received FDA 510(k) clearance on 2003-01-29. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K023659.

When did 1-CCD ENDOCAM 5520 SYSTEM receive FDA 510(k) clearance?

1-CCD ENDOCAM 5520 SYSTEM received FDA 510(k) clearance on 2003-01-29, under 510(k) number K023659.

Who is the listed applicant for 1-CCD ENDOCAM 5520 SYSTEM?

The FDA 510(k) record lists Richard Wolf Medical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 1-CCD ENDOCAM 5520 SYSTEM?

The FDA product code for 1-CCD ENDOCAM 5520 SYSTEM is FET.

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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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