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510(k) K850962

OPHTHALMIC DROPPER BOTTLES by Acacia, Inc.

K850962 is an FDA 510(k) premarket notification submitted by Acacia, Inc. for the device "OPHTHALMIC DROPPER BOTTLES". The FDA issued a decision of Substantially Equivalent on March 21, 1985. Acacia, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 21, 1985
Date Received
March 8, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Acacia, Inc.

  • K142527 — Extension Set with BD Q-Syte Luer Access Split Septum (September 19, 2014)
  • K122449 — ENTERAL NUTRITION WARMER (June 13, 2013)
  • K111381 — MEDI-SIS SYRINGE INFUSION SYSTEM (January 13, 2012)
  • K103165 — BLOOD SAMPLING SET (November 10, 2010)
  • K092986 — ACACIA PISTON SYRINGE (October 27, 2009)
  • K972538 — FLOW-EZE BLUNT CANNULA (1999BC) (July 15, 1998)
  • K931095 — SPRING LOADED SYRINGE (September 16, 1993)
  • K912771 — ACACIAS PHARM/PUMP (February 14, 1992)
  • K901063 — LUER LOCK TRANSFER PIN (July 6, 1990)
  • K896990 — PHARMULATOR (March 23, 1990)

FDA data resources