Aries Medical, Inc.
Aries Medical, Inc. appears in FDA public data with 0 recalls, 19 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 28, 1991.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 19
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| 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 |
| K870189 | ARIES TAPERED SHEATH | March 16, 1987 |
| K863185 | 40CC PERCUTANEOUS FURL SINGLE INTRA-AORTIC BALLOON | January 16, 1987 |
| K844220 | ARIES MEDICAL PERFLEX PERCUTANEOUS 40CC D/L BALLOO | February 20, 1985 |
| K850111 | AIRES TUOHY NEEDLES 17GA. X 4 1/2 | January 24, 1985 |
| K842004 | PERCUTANEOUS CATHETER INTRODUCER SET | July 13, 1984 |
| K833632 | ARIES MEDICAL MODEL 700 | May 16, 1984 |
| K840201 | EPIDURAL CATHETER TRAY | March 2, 1984 |
| K840202 | EPIDURAL CATHETER | February 27, 1984 |
| K840641 | VESSEL DILATOR | February 14, 1984 |