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

CALYPSO 4D LOCALIZATION SYSTEM

K Number: K060906 · Decision Jul 28, 2006
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
733
Applicant Total
5
Review Days
116

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
CALYPSO 4D LOCALIZATION SYSTEM
K Number
K060906
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Calypso Medical Technologies, Inc.
Date Received
April 3, 2006
Decision Date
July 28, 2006
Product Code
IYE
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
IYE Accelerator, Linear, Medical

Similar 510(k) Clearances

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

View all

Other Clearances by Calypso Medical Technologies, Inc.

K Number Device Name
K112841 SURFACE BEACON TRANSPONDERS
K112768 CALYPSO SYSTEMS WITH DYNAMIC EDGE GATING
K102373 CALYPSO SYSTEM WITH DYNAMIC EDGE GATING
K080726 CALYPSO 4D LOCALIZATION SYSTEM