510(k) K103817

Device: POSEY BED
Applicant: J. T. POSEY CO.
510(k) number: K103817
Product code: OYS
Decision: Substantially Equivalent (SESE)
Decision date: 2011-04-22
Date received: 2010-12-29
Regulation: 880.6760
Classification name: Patient Bed With Canopy/restraints
Medical specialty: General Hospital
Review panel: General Hospital
Device class: 1
Clearance type: Traditional
Statement or summary: Summary
Third party reviewed: No

Applicant Contact#

Contact: ROBERT KELLEHER
Address: 5635 Peck Rd. Arcadia CA US 91006 91006

FDA Registration Numbers#

3010699203
3014268229
3008061384
3031564213
3006795806
3008830652
3016541541
2182318
3018490352
3008431074
3011389091

Source Documents#

Other 510(k) Records For Product Code OYS #

510(k), Device, Applicant table
510(k)	Device	Applicant	Decision date
K113355	POSEY BED	J. T. Posey Co.	2012-05-02
K113357	POSEY BED	J. T. Posey Co.	2012-03-21

Legacy Summary#

summary

FDA Review#

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