Gynecare Morcellex Tissue Morcellator, Models MX0100 and MX0100R

FDA 510(k) K061050 · ETHICON, Inc.

Substantially Equivalent

510(k) numberK061050

Submission

Device name
Gynecare Morcellex Tissue Morcellator, Models MX0100 and MX0100R
Applicant
ETHICON, Inc.
Somerville, NJ, US
Received
April 17, 2006
Decision date
July 14, 2006
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HET – Laparoscope, Gynecologic (And Accessories)
Device class
Class II (moderate risk)
Regulation
21 CFR 884.1720
Specialty
Obstetrics/Gynecology

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Questions and answers

When was Gynecare Morcellex Tissue Morcellator, Models MX0100 and MX0100R cleared by the FDA?

Gynecare Morcellex Tissue Morcellator, Models MX0100 and MX0100R (K061050) received a 510(k) decision of Substantially Equivalent on July 14, 2006, 88 days after the submission was received.

What is the product code of K061050?

The FDA product code is HET – Laparoscope, Gynecologic (And Accessories), a Class II (moderate risk) device regulated under 21 CFR 884.1720.