510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
MHCClass II

Needle, Interosseous

21 CFR 880.5570 / General Hospital
FDA source (opens on fda.gov)

MHC is the FDA product code for Needle, Interosseous, a class II device type, regulated under 21 CFR 880.5570. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
MHC
Device name
Needle, Interosseous
Regulation
21 CFR 880.5570
Device class
Class II
Review panel
General Hospital
Submission type
510(k)
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
2
Ingested recalls
0

Clearances, product code MHC

By decision year
2 clearances under product code MHC with a decision year between 2021 and 2022, 2021 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MHC by decision year
YearClearances
20211
20221

Applicants with the most clearances

Product code MHC
Applicants holding the most 510(k) clearances under product code MHC
ApplicantClearances
Bard Access Systems, Inc.1
Bard Access Systems, Inc(Bas)[Wholly-Owned Subsidiary of BD]1

Companies listing this code with FDA

Companies whose registered establishments list this code