Olympus FG-45/46-1 Grasping Forceps(Urology)

FDA 510(k) K962387 · Olympus America, Inc.

Substantially Equivalent

510(k) numberK962387

Submission

Device name
Olympus FG-45/46-1 Grasping Forceps(Urology)
Applicant
Olympus America, Inc.
Melville, NY, US
Received
June 20, 1996
Decision date
July 31, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FFL – Dislodger, Stone, Basket, Ureteral, Metal
Device class
Class II (moderate risk)
Regulation
21 CFR 876.4680
Specialty
Gastroenterology, Urology

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Questions and answers

When was Olympus FG-45/46-1 Grasping Forceps(Urology) cleared by the FDA?

Olympus FG-45/46-1 Grasping Forceps(Urology) (K962387) received a 510(k) decision of Substantially Equivalent on July 31, 1996, 41 days after the submission was received.

What is the product code of K962387?

The FDA product code is FFL – Dislodger, Stone, Basket, Ureteral, Metal, a Class II (moderate risk) device regulated under 21 CFR 876.4680.