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

SEGURA BASKET

K Number: K841942 · Decision Jul 19, 1984
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
51
Applicant Total
52
Review Days
69

Basic Information

Device Name
SEGURA BASKET
K Number
K841942
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.4680
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
VAN-TEC, INC.
Date Received
May 11, 1984
Decision Date
July 19, 1984
Product Code
FFL
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
FFL Dislodger, Stone, Basket, Ureteral, Metal

Similar 510(k) Clearances

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

View all

Other Clearances by VAN-TEC, INC.

K Number Device Name
K880098 VAN-TEC AUTO BIOPSY NEEDLE
K880096 VAN-TEC ASPIRATION BIOPSY SYSTEM W/COLLECTION CUP
K880095 BERGER PROSTATE CULTURE CYTOLOGY BRUSH
K880099 VAN-TEC BLADDER EVACUATOR
K880094 VAN-TEC ENDOPYELOTOMY KNIFE
K874112 VAN-TEC DOUBLE OCCLUSION BALLOON CATHETER
K871777 VAN-TEC REUSABLE HELICAL STONE BASKET
K871779 HELICAL STONE BASKET (DISPOSABLE)
K870696 VAN-TEC SEGURA STONE BASKET W/PROTECTIVE SHEATH
K870679 VAN-TEC MODULAR FLEXIBLE CYSTOURETHROSCOPE
Search all 52 clearances from VAN-TEC, INC. →