Advance Medical Device, Inc.
Ontario L3y 4v8, Canada, CA
Advance Medical Device, Inc. appears in FDA device records in Ontario L3y 4v8, Canada, CA. FDA records list 5 510(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
- 5
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 5 510(k) clearances for Advance Medical Device, Inc. between 1990 and 1997. The busiest year on record is 1991, with 2. The most recent is 1997, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1990 | 1 |
| 1991 | 2 |
| 1995 | 1 |
| 1997 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K964697 | AMD HOME HEALTH MONITOR SYSTEM AND AMD MONITORING STATION | DXN | Substantially Equivalent | |
| K943200 | FLOSCOPE SUPER VASCULAR LAB | JAF | Substantially Equivalent | |
| K910441 | FLOSCOPE MICRODOP | DPT | Substantially Equivalent | |
| K905157 | FLOSCOPE VASCULAR LAB. | JOP | Substantially Equivalent | |
| K903744 | PHYSICIAN'S CHOICE | HIB | 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