Moss Tubes, Inc. Nasal Tube - Mark IV

FDA 510(k) K984629 · Moss Tubes, Inc.

Substantially Equivalent

510(k) numberK984629

Submission

Device name
Moss Tubes, Inc. Nasal Tube - Mark IV
Applicant
Moss Tubes, Inc.
Elizabeth, NJ, US
Received
December 30, 1998
Decision date
March 2, 1999
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

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

Other 510(k)s with product code BSS

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K142483TurboSEAL Nasogastric Aspiration TubeBSS · Traditional Turboseal, L.P.12/19/2014SE
K051480Enteral Feeding TubeBSS · Traditional Biosearch Medical Products, Inc.10/12/2005SE
K961711Aspisafe Gastric TubeBSS · Traditional B.Braun Medical, Inc.06/11/1997SE
K933596Gastric, Catheter, Irrigation & AspirationBSS · Traditional Polamedco, Inc.02/13/1995SE
K930510Radius Enteral Feeding TubeBSS · Traditional Radius Intl., Inc.02/01/1995SE
K935688AN-10S Andersen Tube with StyletBSS · Traditional H.W. Andersen Products, Inc.12/30/1994SE
K934348Tri-Med Quick-Step Gastric Lavage Tube Sizes 18FR, 22FR, 32FRBSS · Traditional Tri-Med Specialties, Inc.12/23/1994SE
K905573Xemex Enteral Nutrition Catheter Nasogas. Type aBSS · Traditional Zeon Medical Corp.06/19/1991SE
K910479Argyle Polyurethane Salem Sump TubeBSS · Traditional Sherwood Medical Co.04/19/1991SE
K894870Wiltek Nasal Biliary Drainage SetBSS · Traditional Wiltek Medical, Inc.12/21/1989SE

More from Wiltek Medical, Inc.

510(k)DeviceDecision
K190414Moss Gastrostomy Tube, Moss Nasal Tube – Mark IVPIF · Special 06/14/2019SE
K990389Moss Gastrostomy TubeKNT · Traditional 03/22/1999SE
K984628Modification of Moss P.E.G. TrayKNT · Traditional 03/17/1999SE
K984310Moss Tubes, Inc, All Silicone Gastrostomy TubeKNT · Traditional 02/24/1999SE

Questions and answers

When was Moss Tubes, Inc. Nasal Tube - Mark IV cleared by the FDA?

Moss Tubes, Inc. Nasal Tube - Mark IV (K984629) received a 510(k) decision of Substantially Equivalent on March 2, 1999, 62 days after the submission was received.

What is the product code of K984629?

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