FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

MIDWEST 1000

K Number: K790113 · Decision Feb 26, 1979
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
260
Applicant Total
13
Review Days
38

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Basic Information

Device Name
MIDWEST 1000
K Number
K790113
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4200
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Midwest
Date Received
January 19, 1979
Decision Date
February 26, 1979
Product Code
EFB
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
EFB Handpiece, Air-Powered, Dental

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