510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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BSSClass II

Tube, Nasogastric

21 CFR 876.5980 / Gastroenterology, Urology
FDA source (opens on fda.gov)

BSS is the FDA product code for Tube, Nasogastric, a class II device type, regulated under 21 CFR 876.5980. As of , FDA records hold 13 510(k) clearances under this code, the most recent dated , and 5 recalls.

Classification record

Product code
BSS
Device name
Tube, Nasogastric
Regulation
21 CFR 876.5980
Device class
Class II
Review panel
Gastroenterology, Urology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
13
Ingested recalls
5

Clearances, product code BSS

By decision year
13 clearances under product code BSS with a decision year between 1979 and 2014, 1989 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code BSS by decision year
YearClearances
19791
19892
19912
19942
19952
19971
19991
20051
20141

Applicants with the most clearances

Product code BSS
Applicants holding the most 510(k) clearances under product code BSS
ApplicantClearances
Abbott Medical1
B.Braun Medical, Inc.1
Biosearch Medical Products, Inc.1
H.W. Andersen Products, Inc.1
Moss Tubes, Inc.1
Polamedco, Inc.1
Radius Intl., Inc.1
Sherwood Medical Co.1
Tecnol New Jersey Wound Care, Inc.1
Tri-Med Specialties, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code