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

MS-III MINISTIM

K Number: K913184 · Decision Oct 7, 1991
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
62
Applicant Total
68
Review Days
81

Basic Information

Device Name
MS-III MINISTIM
K Number
K913184
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2775
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
LIFE-TECH INTL., INC.
Date Received
July 18, 1991
Decision Date
October 7, 1991
Product Code
BXN
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
BXN Stimulator, Nerve, Battery-Powered

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