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

VISITEC NEEDLE RANGE (ANESTHESIOLOGY)

K Number: K811963 · Decision Jul 16, 1981
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
151
Applicant Total
49
Review Days
6

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Basic Information

Device Name
VISITEC NEEDLE RANGE (ANESTHESIOLOGY)
K Number
K811963
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5150
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Visitec Co.
Date Received
July 10, 1981
Decision Date
July 16, 1981
Product Code
BSP
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
BSP Needle, Conduction, Anesthetic (W/Wo Introducer)

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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
Search all 49 clearances from Visitec Co. →