FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

Diros OWL Sterile Single Use TridentTM R.F. Insulated Cannulae,Models DTR and DTRH

K Number: K150371 · Decision Jul 30, 2015
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
65
Applicant Total
8
Review Days
167

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Basic Information

Device Name
Diros OWL Sterile Single Use TridentTM R.F. Insulated Cannulae,Models DTR and DTRH
K Number
K150371
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4725
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Diros Technology, Inc.
Date Received
February 13, 2015
Decision Date
July 30, 2015
Product Code
GXI
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
GXI Probe, Radiofrequency Lesion

Similar 510(k) Clearances

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

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Other Clearances by Diros Technology, Inc.

K Number Device Name
K170708 OWL RF INSULATED CANNULAE
K141586 OWL CANNULAE
K102566 OWL CANNULAE
K110593 OWL RF PROBES
K093185 OWL UNIVERSAL RF SYSTEM URF-3AP (ML)
K062758 OWL URF-3AP
K021869 OWL RADIOFREQUENCY SYSTEM, MODEL URF-2AP