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510(k) K003511

Device
KENDALL-LTP TURNER SAVE-A-LINE
Applicant
The Ludlow Company LP
510(k) number
K003511
Product code
FRP
Decision
Substantially Equivalent (SESE)
Decision date
2001-01-24
Date received
2000-11-14
Regulation
880.5680
Classification name
Holder, Infant Position
Medical specialty
General Hospital
Review panel
General Hospital
Device class
1
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
KATHLEEN M MURPHY
Address
Two Ludlow Park Chicopee MA US 01022 01022

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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