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

ANTRUM & ATTIC MIRROR

K Number: K833601 · Decision Jan 3, 1984
Classifications
1
FEI Numbers
106
Registration Numbers
106
Same Product Code
8
Applicant Total
24
Review Days
83

Basic Information

Device Name
ANTRUM & ATTIC MIRROR
K Number
K833601
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.4420
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
MICROTEK MEDICAL, INC.
Date Received
October 12, 1983
Decision Date
January 3, 1984
Product Code
KAI
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

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

Product Code Device Name
KAI Mirror, Ent

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