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

VICO MICRO SURGICAL INSTRUMENTS

K Number: K843592 · Decision Oct 5, 1984
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
8
Applicant Total
49
Review Days
23

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Basic Information

Device Name
VICO MICRO SURGICAL INSTRUMENTS
K Number
K843592
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.4540
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Visitec Co.
Date Received
September 12, 1984
Decision Date
October 5, 1984
Product Code
HWQ
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
HWQ Passer

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Other Clearances by Visitec Co.

K Number Device Name
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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
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