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

FASTUBE NERVE REGENERATION DEVICE

K Number: K850785 · Decision Jul 10, 1985
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
39
Applicant Total
35
Review Days
134

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Basic Information

Device Name
FASTUBE NERVE REGENERATION DEVICE
K Number
K850785
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5275
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Research Medical, Inc.
Date Received
February 26, 1985
Decision Date
July 10, 1985
Product Code
JXI
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
JXI Cuff, Nerve

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K960098 RMI INTERNAL MAMMARY ARTERY CANNULA
K951344 RMI HEMOCONCENTRATOR
K922083 RMI SURGICCAL SITE VISUALIZATION WAND
K920936 RMI EXTERNAL CORONARY ARTERY OCCLUDER
K915869 RMI NORMOCLUDER CORONARY ARTERY OCCLUDER
K920676 RMI SOFCLAMP
K910221 RMI VASCULAR TOURNIQUET KIT
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