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

FIBER MESH

K Number: K854977 · Decision Feb 20, 1986
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
6
Review Days
70

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Basic Information

Device Name
FIBER MESH
K Number
K854977
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Pulpdent Corp. of America
Date Received
December 12, 1985
Decision Date
February 20, 1986
Product Code
DZE
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
DZE Implant, Endosseous, Root-Form

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K853447 POLYCARB WATER SET
K810545 PCA PERIOCARE PERIODONTAL DRESSING