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510(k) K840641

VESSEL DILATOR by Aries Medical, Inc.

K840641 is an FDA 510(k) premarket notification submitted by Aries Medical, Inc. for the device "VESSEL DILATOR". The FDA issued a decision of SESP on February 14, 1984. Aries Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESP ()
Decision Date
February 14, 1984
Date Received
February 14, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Aries Medical, Inc.

  • K912604 — SJM/CAD ISOFLOW(TM) CENTRIFUGAL PUMP 2100CP, MODIF (October 28, 1991)
  • K903925 — ARIES MELDICAL MODEL 2100HC HANK CRANK (December 21, 1990)
  • K903442 — ARIES TAPERSEAL(TM) SHEATH (August 23, 1990)
  • K895433 — ARIES 30CC & 50CC INTRA-AORTIC BALLOON & CONT. SYS (April 10, 1990)
  • K882289 — ARIES 40CC PERCU. (D/L) INTRA-AORTIC BALLOON CATH. (December 12, 1988)
  • K864537 — 40CC PERCUTANEOUS PRE-FURL (D/L) BALLOON CATHETER (June 19, 1987)
  • K864994 — 40CC PER. PRE-FURL (S/L) INTRA-AORTIC CATHETER (June 19, 1987)
  • K864568 — 40CC SURGICAL DOUBLE LUMEN BALLOON CATHETER (May 12, 1987)
  • K864567 — 40CC PERCUTANEOUS FURL DOU. LUMEN BALLOON CATHETER (May 12, 1987)
  • K871140 — ARIES PEEL AWAY PERCUTANEOUS CATHETER INTRODUCER (April 22, 1987)

FDA data resources