9 French 42LONG Polyurethane Graduated Enteric Fe

FDA 510(k) K843975 · Superior Plastic Products Corp.

Substantially Equivalent

510(k) numberK843975

Submission

Device name
9 French 42LONG Polyurethane Graduated Enteric Fe
Applicant
Superior Plastic Products Corp.
Cumberland, RI, US
Received
October 11, 1984
Decision date
November 20, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KNT – Tubes, Gastrointestinal (And Accessories)
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5980
Specialty
Gastroenterology, Urology

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K242901ZZIREN™ Orogastric Tube; ZZIREN™ SGT Orogastric Tube - 32 Fr (ZZ-SGT-32); ZZIREN™ SGT…KNT · Traditional Tools For Surgery, LLC01/10/2025SE
K241169Entarik NI Feeding Tube SystemKNT · Traditional Gravitas Medical, Inc.11/22/2024SE
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K233591StylusKNT · Traditional Degania Silicone , Ltd.05/31/2024SE

More from Degania Silicone , Ltd.

510(k)DeviceDecision
K851981No. 5300-3 1/2 French Umbilical Vessel Cath. Etc.FOZ · Traditional 06/18/1985SE
K841945Enteral Feeding BottleKNT · Traditional 07/26/1984SE
K841630Enteral Nutrition PumpFRN · Traditional 06/07/1984SE
K841480Infection Control ValveBSY · Traditional 04/25/1984SE
K840324Silicone Sump Drain 20 & 40 FrenchJCY · Traditional 04/25/1984SE
K840323Silicone Suction & Irrigation DrainGBX · Traditional 04/25/1984SE
K833687Dispos. Enteric Feeding Tubes W/Safe-TKNT · Traditional 03/02/1984SE
K833947Superior Enternal Feeding SystemKNT · Traditional 02/04/1984SE
K8204603.5 & 5.5 Oz. Sodium Chloride SolutionJOL · Traditional 03/08/1982SE
K812312Sterile Water 4OZ.JOL · Traditional 11/13/1981SE

Questions and answers

When was 9 French 42LONG Polyurethane Graduated Enteric Fe cleared by the FDA?

9 French 42LONG Polyurethane Graduated Enteric Fe (K843975) received a 510(k) decision of Substantially Equivalent on November 20, 1984, 40 days after the submission was received.

What is the product code of K843975?

The FDA product code is KNT – Tubes, Gastrointestinal (And Accessories), a Class II (moderate risk) device regulated under 21 CFR 876.5980.