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

9075

K Number: K760418 · Decision Aug 23, 1976
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
130
Applicant Total
29
Review Days
14

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Basic Information

Device Name
9075
K Number
K760418
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3765
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Lee Pharmaceuticals
Date Received
August 9, 1976
Decision Date
August 23, 1976
Product Code
EBC
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
EBC Sealant, Pit And Fissure, And Conditioner

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Other Clearances by Lee Pharmaceuticals

K Number Device Name
K924378 RESTOBOND 4
K912256 PRECISE(R) BETA QUARTZ GLASS-CERAMIC INSERT
K900809 LEE-FISCHER CERAMIC REINFORCED PLASTIC BRACKETS
K894315 RESTOBOND 3/DENTIN-ENAMEL BONDING AGENT
K881903 PROSTHODENT VL
K873123 LEE COMPOSITE INLAY SYSTEM
K863157 RESTODENT POSTERIOR
K854882 PROTEC/VISIBLE LIGHT-CURED SEALANT/DENTAL RESTORAT
K844133 CLEANSE N BOND I
K844134 CLEANSE N BOND II
Search all 29 clearances from Lee Pharmaceuticals →