510(k) K895432

Device
Safe-t-cap
Applicant
AUSMEDICS PTY LTD.
510(k) number
K895432
Product code
FMI
Decision
Substantially Equivalent (SESE)
Decision date
1989-11-03
Date received
1989-09-08
Regulation
880.5570
Classification name
Needle, Hypodermic, Single Lumen
Medical specialty
General Hospital
Review panel
General Hospital
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
PAUL M HYMAN
Address
1120 G. St. NW Washington DC US 20005 20005

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

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