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FDA 510(k)

ENDOSCOPIC HYSTERECTOMY AND UTERUS MANIPULATOR

K-Number: K964276 · 1997-11-25

ApplicantRichard Wolf Medical Instruments Corp.
Decision Date1997-11-25
Product CodeHEW
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ENDOSCOPIC HYSTERECTOMY AND UTERUS MANIPULATOR 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 1997-11-25 under 510(k) number K964276. The device is classified under product code HEW. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOSCOPIC HYSTERECTOMY AND UTERUS MANIPULATOR?

ENDOSCOPIC HYSTERECTOMY AND UTERUS MANIPULATOR is a medical device that received FDA 510(k) clearance on 1997-11-25. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K964276.

When did ENDOSCOPIC HYSTERECTOMY AND UTERUS MANIPULATOR receive FDA 510(k) clearance?

ENDOSCOPIC HYSTERECTOMY AND UTERUS MANIPULATOR received FDA 510(k) clearance on 1997-11-25, under 510(k) number K964276.

Who is the listed applicant for ENDOSCOPIC HYSTERECTOMY AND UTERUS MANIPULATOR?

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 ENDOSCOPIC HYSTERECTOMY AND UTERUS MANIPULATOR?

The FDA product code for ENDOSCOPIC HYSTERECTOMY AND UTERUS MANIPULATOR is HEW.

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Related Devices (Code: HEW)

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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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