16 Long Catheter W/Adapter, 14 FR and 12 FR

FDA 510(k) K885202 · Coeur Laboratories, Inc.

Substantially Equivalent

510(k) numberK885202

Submission

Device name
16 Long Catheter W/Adapter, 14 FR and 12 FR
Applicant
Coeur Laboratories, Inc.
Raleigh, NC, US
Received
December 16, 1988
Decision date
January 31, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KOD – Catheter, Urological
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5130
Specialty
Gastroenterology, Urology

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K890292PCA-10, 10CC Disp. Angiography Control SyringeDXT · Traditional 06/22/1989SE
K885138Capillary Tube, Blood CollectionGIO · Traditional 02/07/1989SE
K881646Urological CatheterKOD · Traditional 06/16/1988SE
K874579Coeur Control SyringeFMF · Traditional 01/19/1988SE
K873597Tubing, PolyethyleneDXT · Traditional 11/12/1987SE
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Questions and answers

When was 16 Long Catheter W/Adapter, 14 FR and 12 FR cleared by the FDA?

16 Long Catheter W/Adapter, 14 FR and 12 FR (K885202) received a 510(k) decision of Substantially Equivalent on January 31, 1989, 46 days after the submission was received.

What is the product code of K885202?

The FDA product code is KOD – Catheter, Urological, a Class II (moderate risk) device regulated under 21 CFR 876.5130.