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

Sling, Overhead Suspension, Wheelchair

21 CFR 890.3910 / Physical Medicine
FDA source (opens on fda.gov)

INE is the FDA product code for Sling, Overhead Suspension, Wheelchair, a class I device type, regulated under 21 CFR 890.3910. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
INE
Device name
Sling, Overhead Suspension, Wheelchair
Regulation
21 CFR 890.3910
Device class
Class I
Review panel
Physical Medicine
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code INE

By decision year
1 clearance under product code INE with a decision year between 1989 and 1989, 1989 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code INE by decision year
YearClearances
19891

Applicants with the most clearances

Product code INE
Applicants holding the most 510(k) clearances under product code INE
ApplicantClearances
Medical Alignment Systems1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 18 companies shown, in name order