FDA 510(k) Substantially Equivalent 🇺🇸 United States

REPLICA BONDING AGENT

K Number: K771881 · Decision Nov 9, 1977
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
11
Review Days
36

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Basic Information

Device Name
REPLICA BONDING AGENT
K Number
K771881
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Hoyt Laboratories
Date Received
October 4, 1977
Decision Date
November 9, 1977
Advisory Committee
Unknown
Review Advisory Committee
DE
Third Party
N

Other Clearances by Hoyt Laboratories

K Number Device Name
K820738 LUSTRALLOY
K811154 HOYT ECONO-TRAY
K810830 HOYT COTTON ROLLS
K780834 PREVI DENT PROPHYLAXIS MINT NDC
K771880 REPLICA DENTAL COMPOSIT
K771883 REPLICA ACID-ETCH
K771882 REPLICA DENTAL COMPOSITE-RADIOPAQUE
K771185 PERIODONTIC TOOTHBRUSH, #0126-0190-00
K771184 TOOTHBRUSH, ORTHODONTIC, #0126-0189-00
K771183 TOOTHBRUSH, PEDODONTIC, #0126-0188-00
Search all 11 clearances from Hoyt Laboratories →