FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

TECA. MILLENNIUM

K Number: K965065 · Decision Jun 20, 1997
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
138
Applicant Total
8
Review Days
184

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Basic Information

Device Name
TECA. MILLENNIUM
K Number
K965065
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1870
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Medelec , Ltd.
Date Received
December 18, 1996
Decision Date
June 20, 1997
Product Code
GWF
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
GWF Stimulator, Electrical, Evoked Response

Similar 510(k) Clearances

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

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Other Clearances by Medelec , Ltd.

K Number Device Name
K964280 DG NERVUS
K954157 DG PORTABLE SYSTEM
K953799 DG EXAMINER PLUS
K953732 TECA PREMIERE
K934670 DG 3P SYSTEM
K934669 ARC
K923303 SAPPHIRE PREMIERE