FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

POSEY BED

K Number: K103817 · Decision Apr 22, 2011
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
2
Applicant Total
13
Review Days
114

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Basic Information

Device Name
POSEY BED
K Number
K103817
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6760
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
J. T. Posey Co.
Date Received
December 29, 2010
Decision Date
April 22, 2011
Product Code
OYS
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OYS Patient Bed With Canopy/Restraints

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OYS), ordered by most recent decision date.

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Other Clearances by J. T. Posey Co.

K Number Device Name
K113355 POSEY BED
K113357 POSEY BED
K963414 MULTIPLE BELTS
K963410 POSEY STRAIGHT JACKETS
K963442 JACKETS AND VESTS
K963436 RESTRAINT ACCESSORIES
K963439 PEDIATRIC LIMB HOLDERS
K963437 PELVIC HOLDERS
K963411 POSEY LAPTOP TRAYS
K963413 MULTIPLE LIMB HOLDERS
Search all 13 clearances from J. T. Posey Co. →