Mammotome HH Hand-Held Probe, Vacuum Set, Control Module, HH Hand-Held Holster and Cables, Software Package, Footswitch,

FDA 510(k) K991980 · Ethicon Endo-Surgery, Inc.

Substantially Equivalent

510(k) numberK991980

Submission

Device name
Mammotome HH Hand-Held Probe, Vacuum Set, Control Module, HH Hand-Held Holster and Cables, Software Package, Footswitch,
Applicant
Ethicon Endo-Surgery, Inc.
Cincinnati, OH, US
Received
June 14, 1999
Decision date
August 17, 1999
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KNW – Instrument, Biopsy
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1075
Specialty
Gastroenterology, Urology

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Questions and answers

When was Mammotome HH Hand-Held Probe, Vacuum Set, Control Module, HH Hand-Held Holster and Cables, Software Package, Footswitch, cleared by the FDA?

Mammotome HH Hand-Held Probe, Vacuum Set, Control Module, HH Hand-Held Holster and Cables, Software Package, Footswitch, (K991980) received a 510(k) decision of Substantially Equivalent on August 17, 1999, 64 days after the submission was received.

What is the product code of K991980?

The FDA product code is KNW – Instrument, Biopsy, a Class II (moderate risk) device regulated under 21 CFR 876.1075.