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

Device, Percutaneous, Biopsy

21 CFR 878.4800 / General, Plastic Surgery
FDA source (opens on fda.gov)

MJG is the FDA product code for Device, Percutaneous, Biopsy, a class I device type, regulated under 21 CFR 878.4800. As of , FDA records hold 7 510(k) clearances under this code, the most recent dated , and 4 recalls.

Classification record

Product code
MJG
Device name
Device, Percutaneous, Biopsy
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
7
Ingested recalls
4

Clearances, product code MJG

By decision year
7 clearances under product code MJG with a decision year between 1993 and 2008, 1993 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code MJG by decision year
YearClearances
19932
19941
19961
19991
20071
20081

Applicants with the most clearances

Product code MJG
Applicants holding the most 510(k) clearances under product code MJG
ApplicantClearances
Bip USA, Inc.1
Buckman Co., Inc.1
Clevex, Inc.1
Contour Fabricators of Florida, Inc.1
Nhr, Inc.1
Pajunk GmbH Medizintechnologie1
Sts Biopolymers1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 58 companies shown, in name order