Ethicon Endo-Surgery Flexible Bipolar Hemostasis Forceps

FDA 510(k) K091259 · Ethicon Endo-Surgery, Inc.

Substantially Equivalent

510(k) numberK091259

Submission

Device name
Ethicon Endo-Surgery Flexible Bipolar Hemostasis Forceps
Applicant
Ethicon Endo-Surgery, Inc.
Cincinnati, OH, US
Received
April 29, 2009
Decision date
January 15, 2010
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GEI – Electrosurgical, Cutting & Coagulation & Accessories
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4400
Specialty
General, Plastic Surgery

Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

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Questions and answers

When was Ethicon Endo-Surgery Flexible Bipolar Hemostasis Forceps cleared by the FDA?

Ethicon Endo-Surgery Flexible Bipolar Hemostasis Forceps (K091259) received a 510(k) decision of Substantially Equivalent on January 15, 2010, 261 days after the submission was received.

What is the product code of K091259?

The FDA product code is GEI – Electrosurgical, Cutting & Coagulation & Accessories, a Class II (moderate risk) device regulated under 21 CFR 878.4400.