FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

VISITEC EYE SHIELD

K Number: K843197 · Decision Oct 5, 1984
Classifications
1
FEI Numbers
172
Registration Numbers
172
Same Product Code
16
Applicant Total
49
Review Days
52

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Basic Information

Device Name
VISITEC EYE SHIELD
K Number
K843197
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4440
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Visitec Co.
Date Received
August 14, 1984
Decision Date
October 5, 1984
Product Code
HMP
Advisory Committee
General, Plastic Surgery
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
HMP Pad, Eye

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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. →