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

Bed, Patient Rotation, Manual

21 CFR 890.5180 / Physical Medicine
FDA source (opens on fda.gov)

INY is the FDA product code for Bed, Patient Rotation, Manual, a class I device type, regulated under 21 CFR 890.5180. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
INY
Device name
Bed, Patient Rotation, Manual
Regulation
21 CFR 890.5180
Device class
Class I
Review panel
Physical Medicine
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code INY

By decision year
1 clearance under product code INY with a decision year between 1985 and 1985, 1985 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code INY by decision year
YearClearances
19851

Applicants with the most clearances

Product code INY
Applicants holding the most 510(k) clearances under product code INY
ApplicantClearances
KCI USA, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code