ClearanceBrief
Company · US

Moss Tubes, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1999 to 2019. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KNTTubes, Gastrointestinal (And Accessories)3
BSSTube, Nasogastric1
PIFGastrointestinal Tubes With Enteral Specific Connectors1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 14, 2019K190414Moss Gastrostomy Tube, Moss Nasal Tube – Mark IV
Moss Tubes, Inc.
PIF
Mar 22, 1999K990389MOSS GASTROSTOMY TUBE
Moss Tubes, Inc.
KNT
Mar 17, 1999K984628MODIFICATION OF MOSS P.E.G. TRAY
Moss Tubes, Inc.
KNT
Mar 2, 1999K984629MOSS TUBES, INC. NASAL TUBE - MARK IV
Moss Tubes, Inc.
BSS
Feb 24, 1999K984310MOSS TUBES, INC, ALL SILICONE GASTROSTOMY TUBE
Moss Tubes, Inc.
KNT

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes