Applied Medical Laparoscopic Linear Cutter

FDA 510(k) K190331 · Applied Medical Resources Corporation

Substantially Equivalent

510(k) numberK190331

Submission

Device name
Applied Medical Laparoscopic Linear Cutter
Applicant
Applied Medical Resources Corporation
Rancho Santa, CA, US
Received
February 14, 2019
Decision date
November 22, 2019
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GDW – Staple, Implantable
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4750
Specialty
General, Plastic Surgery
Implant
Yes

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Questions and answers

When was Applied Medical Laparoscopic Linear Cutter cleared by the FDA?

Applied Medical Laparoscopic Linear Cutter (K190331) received a 510(k) decision of Substantially Equivalent on November 22, 2019, 281 days after the submission was received.

What is the product code of K190331?

The FDA product code is GDW – Staple, Implantable, a Class II (moderate risk) device regulated under 21 CFR 878.4750.