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

CYSTOTOMES

K Number: K790244 · Decision Feb 12, 1979
Classifications
1
FEI Numbers
80
Registration Numbers
81
Same Product Code
19
Applicant Total
49
Review Days
45

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Basic Information

Device Name
CYSTOTOMES
K Number
K790244
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4350
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Visitec Co.
Date Received
December 29, 1978
Decision Date
February 12, 1979
Product Code
HNY
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
HNY Cystotome

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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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