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
OYSClass I

Patient Bed With Canopy/Restraints

21 CFR 880.6760 / General Hospital
FDA source (opens on fda.gov)

OYS is the FDA product code for Patient Bed With Canopy/Restraints, a class I device type, regulated under 21 CFR 880.6760. FDA's definition for this code reads: "Enclosed bed canopy system used as passive restraint". As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
OYS
Device name
Patient Bed With Canopy/Restraints
FDA definition
Enclosed bed canopy system used as passive restraint.
Regulation
21 CFR 880.6760
Device class
Class I
Review panel
General Hospital
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
3
Ingested recalls
1

Clearances, product code OYS

By decision year
3 clearances under product code OYS with a decision year between 2011 and 2012, 2012 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code OYS by decision year
YearClearances
20111
20122

Applicants with the most clearances

Product code OYS
Applicants holding the most 510(k) clearances under product code OYS
ApplicantClearances
J. T. Posey Co.3

Companies listing this code with FDA

Companies whose registered establishments list this code