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

VISITEC MICROSURGICAL SUTURE

K Number: K922530 · Decision Oct 20, 1992
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
56
Applicant Total
49
Review Days
145

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Basic Information

Device Name
VISITEC MICROSURGICAL SUTURE
K Number
K922530
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.5020
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Visitec Co.
Date Received
May 28, 1992
Decision Date
October 20, 1992
Product Code
GAR
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
GAR Suture, Nonabsorbable, Synthetic, Polyamide

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GAR), ordered by most recent decision date.

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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
K923645 VISITEC ASPIRATING SYRINGE
Search all 49 clearances from Visitec Co. →