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FDA 510(k)

CCD ENDOCAM 5501

K-Number: K950502 · 1995-05-04

ApplicantRichard Wolf Medical Instruments Corp.
Decision Date1995-05-04
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CCD ENDOCAM 5501 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 1995-05-04 under 510(k) number K950502. 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 CCD ENDOCAM 5501?

CCD ENDOCAM 5501 is a medical device that received FDA 510(k) clearance on 1995-05-04. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K950502.

When did CCD ENDOCAM 5501 receive FDA 510(k) clearance?

CCD ENDOCAM 5501 received FDA 510(k) clearance on 1995-05-04, under 510(k) number K950502.

Who is the listed applicant for CCD ENDOCAM 5501?

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 CCD ENDOCAM 5501?

The FDA product code for CCD ENDOCAM 5501 is GCJ.

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Other records listing Richard Wolf Medical Instruments Corp. as applicant

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Related Devices (Code: GCJ)

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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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