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

Marker, Colon

21 CFR 876.1500 / Gastroenterology, Urology
FDA source (opens on fda.gov)

NBG is the FDA product code for Marker, Colon, a class II device type, regulated under 21 CFR 876.1500. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
NBG
Device name
Marker, Colon
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
2
Ingested recalls
0

Clearances, product code NBG

By decision year
2 clearances under product code NBG with a decision year between 2000 and 2005, 2000 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code NBG by decision year
YearClearances
20001
20051

Applicants with the most clearances

Product code NBG
Applicants holding the most 510(k) clearances under product code NBG
ApplicantClearances
Chek-Med Systems1
PMT Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code