510(k) K010038

Device
NEEDLE BARN STICK STOPPER WITH SAFETY CAP, IN KIT WITH STERILE FIELD DRAPE
Applicant
Cambridge Marketing, Inc.
510(k) number
K010038
Product code
FMI
Decision
Substantially Equivalent (SESE)
Decision date
2001-01-24
Date received
2001-01-05
Regulation
880.5570
Classification name
Needle, Hypodermic, Single Lumen
Medical specialty
General Hospital
Review panel
General Hospital
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
N

Applicant Contact#

Contact
JOSEPH B DUNN
Address
P.O. 306 813 Ela Ave. Waterford WI US 53185 53185

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

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