Angiomedics, Inc.
Walker, MI, US
Angiomedics, Inc. appears in FDA device records in Walker, MI. FDA records list 8 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 8
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 8 510(k) clearances for Angiomedics, Inc. between 1984 and 1987. The busiest year on record is 1987, with 4. The most recent is 1987, with 4.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1984 | 1 |
| 1985 | 2 |
| 1986 | 1 |
| 1987 | 4 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K873195 | SCHNEIDER-SHILEY ANGIOPORT(TM) PTCA INTRO W/HEMO | DYB | Substantially Equivalent | |
| K872542 | SCHNEIDER-SHILEY SOFTRAC-PTA(TM) ANGIO. CATHETER | LIT | Substantially Equivalent | |
| K872472 | SCHNEIDER-SHILEY BIFLATOR BALLOON INFLATION DEVICE | DXT | Substantially Equivalent | |
| K863342 | SOFTIP CORONARY SINUS CARDIOPLEGIA CATHETER | DWF | Substantially Equivalent | |
| K861238 | ANGIOMEDICS CATH SHEATH INTRODUC W/HEMOSTASIS VALV | DYB | Substantially Equivalent | |
| K852872 | ANGIOMEDICS SOFTIP CATHETER | DQO | Substantially Equivalent | |
| K850271 | ANGIOMEDIC'S CATHETER-DIAGNOSTIC INTRAVASCULAR | DQO | Substantially Equivalent | |
| K834275 | SOFTIP CATHETER | DQO | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain