FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

SNM FIRMGRIP

K Number: K092629 · Decision Sep 25, 2009
Classifications
1
FEI Numbers
204
Registration Numbers
205
Same Product Code
503
Applicant Total
4
Review Days
29

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
SNM FIRMGRIP
K Number
K092629
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
880.5200
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Flexicath , Ltd.
Date Received
August 27, 2009
Decision Date
September 25, 2009
Product Code
FOZ
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
FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

Similar 510(k) Clearances

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

View all

Other Clearances by Flexicath , Ltd.

K Number Device Name
K111939 M/29TM - PRESSURE INJECTABLE
K080793 FIRMGRIP
K063363 FIRMGRIP PERIPHERALLY INSERTED CATHETER DEVICE