FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

PICC INSERTION KIT/P.I.C. & PICC EXCHANG KIT/P.E.K

K Number: K910315 · Decision Apr 5, 1991
Classifications
1
FEI Numbers
90
Registration Numbers
90
Same Product Code
301
Applicant Total
9
Review Days
71

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
PICC INSERTION KIT/P.I.C. & PICC EXCHANG KIT/P.E.K
K Number
K910315
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5970
Medical Specialty
General Hospital
Decision
Unknown
Applicant
Sorex Medical
Date Received
January 24, 1991
Decision Date
April 5, 1991
Product Code
LJS
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

Similar 510(k) Clearances

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

View all

Other Clearances by Sorex Medical

K Number Device Name
K923843 FOGLESS
K913036 PLUME MASTER
K911070 PICC-FIX
K911150 SOREX SAFE-AIR
K905572 EDLICH WOUND MANAGEMENT TRAY
K903740 TRACH-EZE
K902410 MEDICAL PROCEDURE TRAY
K885136 GRAFT GUARD