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510(k) K802262

COMPOSITE RESTORATIVE by L.D. Caulk Co.

K802262 is an FDA 510(k) premarket notification submitted by L.D. Caulk Co. for the device "COMPOSITE RESTORATIVE". The FDA issued a decision of SESP on September 16, 1980. L.D. Caulk Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESP ()
Decision Date
September 16, 1980
Date Received
September 16, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by L.D. Caulk Co.

  • K801690 — VALIANT (August 13, 1980)
  • K790585 — FINESSE (May 16, 1979)
  • K790586 — CHEMBOND (May 16, 1979)
  • K780560 — DENTAL AMALGAMATOR (April 21, 1978)
  • K780384 — IMPROVED DYCAL (March 15, 1978)
  • K780301 — CAULK TYLOK (February 28, 1978)
  • K771402 — NUVA-COTE (MODIFICATION TO) (August 26, 1977)
  • K771398 — SHELL VENEER (August 26, 1977)
  • K771399 — LIP & CHEEK RETRACTOR (August 26, 1977)
  • K771401 — PROPHY PASTE (August 22, 1977)

FDA data resources