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

CRW-1 SYSTEM

K Number: K944463 · Decision Oct 26, 1995
Classifications
1
FEI Numbers
250
Registration Numbers
250
Same Product Code
422
Applicant Total
12
Review Days
409

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Basic Information

Device Name
CRW-1 SYSTEM
K Number
K944463
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Radionics Software Applications, Inc.
Date Received
September 12, 1994
Decision Date
October 26, 1995
Product Code
HAW
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
HAW Neurological Stereotaxic Instrument

Similar 510(k) Clearances

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

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Other Clearances by Radionics Software Applications, Inc.

K Number Device Name
K990326 OPTICAL TRACKING SYSTEM MICROSCOPE MODULE II, MODEL OTS MMII
K974602 OPTICAL TRACKING SYSTEM (OTS)
K972905 XPLAN-1
K964801 OPTICAL TRACKING SYSTEM (OTS)
K961844 OPERATING ARM SYSTEM (OAS) [WITH CT AND MR IMAGES]
K962155 GILL-THOMAS-COSMAN(GTC) DENTAL TRAY
K960071 IMAGEFUSION
K951262 OPERATING ARM SYSTEM (OAS)
K953482 XKNIFE-3
K946252 STEREOPLAN
Search all 12 clearances from Radionics Software Applications, Inc. →