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

LEE-FISCHER CERAMIC REINFORCED PLASTIC BRACKETS

K Number: K900809 · Decision Jun 28, 1990
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
41
Applicant Total
29
Review Days
127

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Basic Information

Device Name
LEE-FISCHER CERAMIC REINFORCED PLASTIC BRACKETS
K Number
K900809
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.5470
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Lee Pharmaceuticals
Date Received
February 21, 1990
Decision Date
June 28, 1990
Product Code
DYW
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
DYW Bracket, Plastic, Orthodontic

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Other Clearances by Lee Pharmaceuticals

K Number Device Name
K924378 RESTOBOND 4
K912256 PRECISE(R) BETA QUARTZ GLASS-CERAMIC INSERT
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
K843363 RESTODENT VL
Search all 29 clearances from Lee Pharmaceuticals →