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

VISITEC NEEDLE RANGE (CARDIOVASCULAR)

K Number: K811964 · Decision Jul 20, 1981
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
50
Applicant Total
49
Review Days
10

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Basic Information

Device Name
VISITEC NEEDLE RANGE (CARDIOVASCULAR)
K Number
K811964
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1390
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Visitec Co.
Date Received
July 10, 1981
Decision Date
July 20, 1981
Product Code
DRC
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DRC Trocar

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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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