L.T.C. Percutaneous Endoscopic Gastrostomy Tube

FDA 510(k) K897181 · Intl. Medical Marketing, Inc.

Unknown

510(k) numberK897181

Submission

Device name
L.T.C. Percutaneous Endoscopic Gastrostomy Tube
Applicant
Intl. Medical Marketing, Inc.
Ridge, NY, US
Received
December 28, 1989
Decision date
March 27, 1990
Decision
Unknown (SESD)
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

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K110853VR Medical Enteral Oral SyringeFPD · Traditional Vr Medical05/13/2011SE
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K101214Guardian ConnectionFPD · Traditional Maulin Medical, LLC07/23/2010SE
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More from Philips Children'S Medical Ventures

510(k)DeviceDecision
K896621L.T.C. Replacement Gastrostomy TubeKCQ · Traditional 03/13/1990SE
K895824L.T.C. Enteral Bag Administration Set W/Pump SetFPD · Traditional 03/13/1990SE
K895957L.T.C. 1000 Urinary Drainage BagKNX · Traditional 10/24/1989SE
K895616L.T.C. Feeding TubeKNT · Traditional 10/24/1989SE

Questions and answers

When was L.T.C. Percutaneous Endoscopic Gastrostomy Tube cleared by the FDA?

L.T.C. Percutaneous Endoscopic Gastrostomy Tube (K897181) received a 510(k) decision of Unknown on March 27, 1990, 89 days after the submission was received.

What is the product code of K897181?

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