FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

VISITEC OPHTHALMIC ASPIRATION UNIT MODEL 100

K Number: K853961 · Decision Dec 13, 1985
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
148
Applicant Total
49
Review Days
79

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Basic Information

Device Name
VISITEC OPHTHALMIC ASPIRATION UNIT MODEL 100
K Number
K853961
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4150
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Visitec Co.
Date Received
September 25, 1985
Decision Date
December 13, 1985
Product Code
HQE
Advisory Committee
Ophthalmic
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
HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered

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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. →