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

CYCLOPAC TENS

K Number: K801855 · Decision Aug 13, 1980
Classifications
1
FEI Numbers
80
Registration Numbers
80
Same Product Code
42
Applicant Total
74
Review Days
9

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Basic Information

Device Name
CYCLOPAC TENS
K Number
K801855
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4800
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Dow Corning Wright
Date Received
August 4, 1980
Decision Date
August 13, 1980
Product Code
GZT
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
GZT Retractor, Self-Retaining, For Neurosurgery

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