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510(k) K863162

VACU-GUARD by Arbor Technologies, Inc.

K863162 is an FDA 510(k) premarket notification submitted by Arbor Technologies, Inc. for the device "VACU-GUARD". The FDA issued a decision of Substantially Equivalent on August 29, 1986. Arbor Technologies, Inc. has at least 9 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 29, 1986
Date Received
August 18, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Arbor Technologies, Inc.

  • K960928 — SYRINGEFILTER (April 4, 1997)
  • K964283 — AUTOPRIME (January 22, 1997)
  • K922777 — PRESSURE TUBING AND ACCESSORIES (March 22, 1994)
  • K902666 — ANESTHESIA CONDUCTION FILTER (April 23, 1991)
  • K895859 — CONTAIN(TM) (February 7, 1991)
  • K902167 — CONTAIN(TM) LASER PLUME FILTER (January 4, 1991)
  • K890844 — MICROSEPT 60/20 (June 7, 1989)
  • K874505 — CONTAIN(TM) (May 20, 1988)
  • K864113 — CLYDE (TM) FILTRATION SYSTEM (February 4, 1987)

FDA data resources