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

URESIL STD FLAT/ROUND & FLAT/ROUND SPLIT. SILI/DRA

K Number: K863560 · Decision Sep 29, 1986
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
26
Applicant Total
45
Review Days
17

Basic Information

Device Name
URESIL STD FLAT/ROUND & FLAT/ROUND SPLIT. SILI/DRA
K Number
K863560
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
URESIL CORP.
Date Received
September 12, 1986
Decision Date
September 29, 1986
Product Code
GBS
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
GBS Catheter, Ventricular, General & Plastic Surgery

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