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510(k) K771881

REPLICA BONDING AGENT by Hoyt Laboratories

K771881 is an FDA 510(k) premarket notification submitted by Hoyt Laboratories for the device "REPLICA BONDING AGENT". The FDA issued a decision of Substantially Equivalent on November 9, 1977. Hoyt Laboratories has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 9, 1977
Date Received
October 4, 1977
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Hoyt Laboratories

  • K820738 — LUSTRALLOY (April 9, 1982)
  • K811154 — HOYT ECONO-TRAY (May 13, 1981)
  • K810830 — HOYT COTTON ROLLS (April 14, 1981)
  • K780834 — PREVI DENT PROPHYLAXIS MINT NDC (June 2, 1978)
  • K771883 — REPLICA ACID-ETCH (October 20, 1977)
  • K771882 — REPLICA DENTAL COMPOSITE-RADIOPAQUE (October 20, 1977)
  • K771880 — REPLICA DENTAL COMPOSIT (October 20, 1977)
  • K771185 — PERIODONTIC TOOTHBRUSH, #0126-0190-00 (July 15, 1977)
  • K771184 — TOOTHBRUSH, ORTHODONTIC, #0126-0189-00 (July 15, 1977)
  • K771183 — TOOTHBRUSH, PEDODONTIC, #0126-0188-00 (July 15, 1977)

FDA data resources