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

TMJ CANNULA SET

K Number: K871648 · Decision Jun 8, 1987
Classifications
1
FEI Numbers
78
Registration Numbers
78
Same Product Code
48
Applicant Total
55
Review Days
41

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Basic Information

Device Name
TMJ CANNULA SET
K Number
K871648
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4120
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Aspen Laboratories, Inc.
Date Received
April 28, 1987
Decision Date
June 8, 1987
Product Code
DZI
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
DZI Drill, Bone, Powered

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