North American Medical Products, Inc.
Albany, NY, US
North American Medical Products, Inc. appears in FDA device records in Albany, NY. FDA records list 6 510(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
- 6
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 6 510(k) clearances for North American Medical Products, Inc. between 1984 and 2001. The busiest year on record is 1984, with 1. The most recent is 2001, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1984 | 1 |
| 1986 | 1 |
| 1989 | 1 |
| 1990 | 1 |
| 1991 | 1 |
| 2001 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K001965 | SAFE-POINT VAC, SAFE-POINT M-D BLOOD COLLECTION SYSTEMS | FMI | Substantially Equivalent | |
| K905305 | SAFE-SITE NEEDLE COVER | FMI | Substantially Equivalent | |
| K895948 | PORT-O-SCOPE(TM) | EOQ | Substantially Equivalent | |
| K896072 | D.L. SCOPE OPHTHALMOSCOPE | HLJ | Substantially Equivalent | |
| K862661 | D.L. SCOPE(R) OTOSCOPE | ERA | Substantially Equivalent | |
| K841778 | D.L. SCOPE BLADE & HANDLE | CCW | 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