(Roth)Spiral Rotating Prostatic Biopsy Needle

FDA 510(k) K863385 · Cook Urological, Inc.

Substantially Equivalent

510(k) numberK863385

Submission

Device name
(Roth)Spiral Rotating Prostatic Biopsy Needle
Applicant
Cook Urological, Inc.
Spencer, IN, US
Received
September 3, 1986
Decision date
November 4, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KNN – Components, Wheelchair
Device class
Class I (low risk)
Regulation
21 CFR 890.3920
Specialty
Physical Medicine

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Questions and answers

When was (Roth)Spiral Rotating Prostatic Biopsy Needle cleared by the FDA?

(Roth)Spiral Rotating Prostatic Biopsy Needle (K863385) received a 510(k) decision of Substantially Equivalent on November 4, 1986, 62 days after the submission was received.

What is the product code of K863385?

The FDA product code is KNN – Components, Wheelchair, a Class I (low risk) device regulated under 21 CFR 890.3920.