Tubing Feeding Kit

FDA 510(k) K770620 · Doyle Pharmaceutical

Substantially Equivalent

510(k) numberK770620

Submission

Device name
Tubing Feeding Kit
Applicant
Doyle Pharmaceutical
Mchenry, IL, US
Received
April 1, 1977
Decision date
May 3, 1977
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FPD – Tube, Feeding
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5980
Specialty
Gastroenterology, Urology

Other 510(k)s with product code FPD

510(k)DeviceApplicantDecision
K243361NutrifitFPD · Traditional Vygon USA12/19/2024SE
K180236VR Medical Feeding Tube and Enteral Feeding Extension Set (EFES)FPD · Traditional Vr Medical Technology Co., Ltd.01/18/2019SE
K131590Innersense Esophageal Temperature Probe / Feeding TubeFPD · Traditional Philips Medical Systems10/23/2013SE
K120815Innersense Esophageal Temperature/Feeding TubeFPD · Traditional Philips Medical Systems03/06/2013SE
K121105Nutrisafe 2 Feeding TubeFPD · Traditional Vygon Corp.12/18/2012SE
K100163Nutrisafe 2 Feeding Tubes Model 362.XXX. 1362.XXXFPD · Traditional Vygon Corp.10/13/2011SE
K110853VR Medical Enteral Oral SyringeFPD · Traditional Vr Medical05/13/2011SE
K100700Med-Rx Pediatric Feeding Tubes and AccessoriesFPD · Traditional Benlan, Inc.12/13/2010SE
K101214Guardian ConnectionFPD · Traditional Maulin Medical, LLC07/23/2010SE
K100099Oral/Enteral SyringesFPD · Traditional Philips Children'S Medical Ventures06/14/2010SE

Questions and answers

When was Tubing Feeding Kit cleared by the FDA?

Tubing Feeding Kit (K770620) received a 510(k) decision of Substantially Equivalent on May 3, 1977, 32 days after the submission was received.

What is the product code of K770620?

The FDA product code is FPD – Tube, Feeding, a Class II (moderate risk) device regulated under 21 CFR 876.5980.