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

VISITEC NEEDLE RANGE (GASTERUROLOGY)

K Number: K811965 · Decision Aug 25, 1981
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
0
Applicant Total
49
Review Days
46

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Basic Information

Device Name
VISITEC NEEDLE RANGE (GASTERUROLOGY)
K Number
K811965
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Visitec Co.
Date Received
July 10, 1981
Decision Date
August 25, 1981
Product Code
FHR
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
FHR Needle, Gastro-Urology

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. →