3 French Flexible Biopsy Forceps

FDA 510(k) K881399 · Cook Urological, Inc.

Substantially Equivalent

510(k) numberK881399

Submission

Device name
3 French Flexible Biopsy Forceps
Applicant
Cook Urological, Inc.
Spencer, IN, US
Received
April 4, 1988
Decision date
April 11, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
OCZ – Endoscopic Grasping/Cutting Instrument, Non-Powered
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

To manually grasp stones, tissues or other objects through an endoscope. To manipulate, sample or cut tissues through an endoscope.

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Questions and answers

When was 3 French Flexible Biopsy Forceps cleared by the FDA?

3 French Flexible Biopsy Forceps (K881399) received a 510(k) decision of Substantially Equivalent on April 11, 1988, 7 days after the submission was received.

What is the product code of K881399?

The FDA product code is OCZ – Endoscopic Grasping/Cutting Instrument, Non-Powered, a Class II (moderate risk) device regulated under 21 CFR 876.1500.