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

RADIOCAMERAS EXTRACRANIAL SYSTEM

K Number: K000246 · Decision Oct 20, 2000
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
733
Applicant Total
27
Review Days
267

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
RADIOCAMERAS EXTRACRANIAL SYSTEM
K Number
K000246
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Surgical Navigation Technologies, Inc.
Date Received
January 27, 2000
Decision Date
October 20, 2000
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 Surgical Navigation Technologies, Inc.

K Number Device Name
K994355 RADIOCAMERAS SYSTEM HEAD/NECK APPLICATION
K992461 STEALTHSTATION TREATMENT GUIDANCE PLATFORM
K992927 STEALTHSTATION TREATMENT GUIDANCE PLATFORM
K993021 METRX SYSTEM
K992354 SNT IMAGE ANALYSIS SYSTEM
K991468 IMMERGE IMAGE CORRELATION
K990214 FLUORONAV MODULE FOR THE STEALTHSTATION SYSTEM
K983670 STEALTHSTATION SYSTEM
K984000 STEALTHSERVER IMAGE STORAGE AND COMMUNICATION SYSTEM
K983397 STEALTHSTATION TREATMENT GUIDANCE PLAFFORM
Search all 27 clearances from Surgical Navigation Technologies, Inc. →