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

VISITEC EYE PAD

K Number: K940210 · Decision Mar 7, 1994
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
270
Applicant Total
49
Review Days
52

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Basic Information

Device Name
VISITEC EYE PAD
K Number
K940210
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Visitec Co.
Date Received
January 14, 1994
Decision Date
March 7, 1994
Product Code
EFQ
Advisory Committee
Unknown
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
EFQ Gauze/Sponge, Internal

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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
K933872 VISI-SPEAR EYE SPONGE
K923972 OPHTHALMIC FLUID DISTRIBUTION SETS
K922530 VISITEC MICROSURGICAL SUTURE
K923645 VISITEC ASPIRATING SYRINGE
Search all 49 clearances from Visitec Co. →