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

HYBRID NERVE LOCATION NEEDLE COATED AND UNCOATED

K Number: K080603 · Decision Aug 5, 2008
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
151
Applicant Total
2
Review Days
155

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Basic Information

Device Name
HYBRID NERVE LOCATION NEEDLE COATED AND UNCOATED
K Number
K080603
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5150
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Te ME NA Sas
Date Received
March 3, 2008
Decision Date
August 5, 2008
Product Code
BSP
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
BSP Needle, Conduction, Anesthetic (W/Wo Introducer)

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Other Clearances by Te ME NA Sas

K Number Device Name
K060186 POLYPLEX STIMULATING CATHETER SYSTEM