510(k) K953394

VISITEC COLLAR BUTTON CATHETER {GRIFFITHS} by Visitec Co. — Product Code LZU

K953394 is an FDA 510(k) premarket notification submitted by Visitec Co. for the device "VISITEC COLLAR BUTTON CATHETER {GRIFFITHS}". The FDA issued a decision of Substantially Equivalent on October 12, 1995. The device falls under product code LZU (Plug, Punctum), a Class U device. Visitec Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 12, 1995
Date Received
July 17, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Plug, Punctum
Device Class
Class U
Regulation Number
Review Panel
OP
Submission Type