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

MICROJET QUARK, MODEL U100 OR U40

K Number: K013807 · Decision Dec 12, 2001
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
83
Applicant Total
10
Review Days
27

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
MICROJET QUARK, MODEL U100 OR U40
K Number
K013807
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cane S.R.L.
Date Received
November 15, 2001
Decision Date
December 12, 2001
Product Code
LZG
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
LZG Pump, Infusion, Insulin

Similar 510(k) Clearances

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

View all

Other Clearances by Cane S.R.L.

K Number Device Name
K091042 CRONO S-PID 50
K052218 CRONO FIVE AND CRONO PCA 50
K052219 CRONO GO.
K052217 CRONO SUPER PID
K042085 CRONO F
K041414 CRONO AND CRONO, MODEL 30
K013840 MICROJET CRONO PAR AND CRONO APO-GO
K013822 MICROJET CRONO PCA
K013234 MICROJET CRONO