FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

VISITEC CANALICULAR STENT

K Number: K915809 · Decision Feb 24, 1992
Classifications
1
FEI Numbers
37
Registration Numbers
38
Same Product Code
48
Applicant Total
49
Review Days
62

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Basic Information

Device Name
VISITEC CANALICULAR STENT
K Number
K915809
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Visitec Co.
Date Received
December 24, 1991
Decision Date
February 24, 1992
Product Code
LZU
Advisory Committee
Unknown
Review Advisory Committee
OP
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LZU Plug, Punctum

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Other Clearances by Visitec Co.

K Number Device Name
K953394 VISITEC COLLAR BUTTON CATHETER {GRIFFITHS}
K945114 VISITEC SCLERAL PLUG
K945738 VISIFLEX OPHTHALMIC SURGICAL INCISE DRAPE
K945172 VISITEC SILICONE RETINAL IMPLANTS/EXPLANTS
K942234 VISITEC PRECISE-POINT
K934269 FIBEROPTIC ILLUMINATED INSTRUMENTS
K940210 VISITEC EYE PAD
K933872 VISI-SPEAR EYE SPONGE
K923972 OPHTHALMIC FLUID DISTRIBUTION SETS
K922530 VISITEC MICROSURGICAL SUTURE
Search all 49 clearances from Visitec Co. →