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

SWAN VALLEY MEDICAL TRANURETHRAL SUPRAPUBIC ENDO-CYSTOSTOMY (T-SPEC) SURGICAL SYSTEM

K Number: K120127 · Decision Oct 26, 2012
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
31
Applicant Total
1
Review Days
283

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
SWAN VALLEY MEDICAL TRANURETHRAL SUPRAPUBIC ENDO-CYSTOSTOMY (T-SPEC) SURGICAL SYSTEM
K Number
K120127
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5090
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Swan Valley Medical, Incorporated
Date Received
January 17, 2012
Decision Date
October 26, 2012
Product Code
KOB
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
KOB Catheter, Suprapubic (And Accessories)

Similar 510(k) Clearances

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

View all