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

SURGERY AND ACCESSORIES

K Number: K021236 · Decision Jul 17, 2002
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
16
Review Days
90

Basic Information

Device Name
SURGERY AND ACCESSORIES
K Number
K021236
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
CAMTRONICS, LTD.
Date Received
April 18, 2002
Decision Date
July 17, 2002
Product Code
LLZ
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
LLZ System, Image Processing, Radiological

Similar 510(k) Clearances

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

View all

Other Clearances by CAMTRONICS, LTD.

K Number Device Name
K013032 PHYSIOLOG, SERIES 95000
K992666 VIDEO PLUS SYSTEM, SERIES 95000
K992259 ECHOCARDIOGRAPHY SYSTEM SERIES 95000
K990066 CCD CAMERA, MODEL 9000
K955519 ANALYTICAL REVIEW STATION
K954159 DIGITAL IMAGING SYSTEM
K955232 NT SERIES DIGITAL IMAGE MANAGER
K953080 DIGITAL IMAGING SYSTEM INTERFACE
K945654 NICOM DIGITAL IMAGE MANAGER
K941979 VIDEO PLUS WITH ANALYTICAL WORKSTATION
Search all 16 clearances from CAMTRONICS, LTD. →