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

BOSWORTH BOND

K Number: K043170 · Decision Feb 25, 2005
Classifications
1
FEI Numbers
137
Registration Numbers
137
Same Product Code
418
Applicant Total
45
Review Days
101

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Basic Information

Device Name
BOSWORTH BOND
K Number
K043170
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3200
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Harry J. Bosworth Co.
Date Received
November 16, 2004
Decision Date
February 25, 2005
Product Code
KLE
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
KLE Agent, Tooth Bonding, Resin

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Other Clearances by Harry J. Bosworth Co.

K Number Device Name
K103585 BOSWORTH AEGIS LINER & RESTORATIVE MATERIAL W/ACP
K100731 BOSWORTH AIR POLISHER
K061611 BOSWORTH DENTIN RESIN
K051224 BOSWORTH SEAL
K040548 AEGIS ORTHO LIGHT-CURED ORTHODONTIC ADHESIVE
K040547 AEGIS ORTHO DUAL-CURED ORTHODONTIC ADHESIVE
K033751 AEGIS PIT & FISSURE SEALANT WITH ACP
K031439 ALGINATE IMPRESSION MATERIAL III (FAST & REGULAR)
K031811 PIT & FISSURE SEALANT WITH FLUORIDE
K994027 ACTIVATOR PASTE
Search all 45 clearances from Harry J. Bosworth Co. →