Endoscopic Hysterectomy and Uterus Manipulator

FDA 510(k) K964276 · Richard Wolf Medical Instruments Corp.

Substantially Equivalent

510(k) numberK964276

Submission

Device name
Endoscopic Hysterectomy and Uterus Manipulator
Applicant
Richard Wolf Medical Instruments Corp.
Vernon Hills, IL, US
Received
October 28, 1996
Decision date
November 25, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HEW – Culdoscope (And Accessories)
Device class
Class II (moderate risk)
Regulation
21 CFR 884.1640
Specialty
Obstetrics/Gynecology

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Questions and answers

When was Endoscopic Hysterectomy and Uterus Manipulator cleared by the FDA?

Endoscopic Hysterectomy and Uterus Manipulator (K964276) received a 510(k) decision of Substantially Equivalent on November 25, 1997, 393 days after the submission was received.

What is the product code of K964276?

The FDA product code is HEW – Culdoscope (And Accessories), a Class II (moderate risk) device regulated under 21 CFR 884.1640.