Pulse Metric, Inc.
San Diego, CA, US
Pulse Metric, Inc. appears in FDA device records in San Diego, 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 Pulse Metric, Inc. between 1991 and 2002. The busiest year on record is 2001, with 2. The most recent is 2002, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1991 | 1 |
| 1995 | 1 |
| 2001 | 2 |
| 2002 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K013478 | DYNAPULSE 5200A PATHWAY BLOOD PRESSURE MONITORING SYSTEM | DXN | Substantially Equivalent | |
| K013358 | DYNAPULSE 5000A MINI ABP BLOOD PRESSURE MONITORING SYSTEM | DXN | Substantially Equivalent | |
| K012498 | DYNAPULSE 500G (DP500G) BLLOD PRESSURE MONITORING SYSTEM | DXN | Substantially Equivalent | |
| K945111 | DYNAPULSE 5000A (DP5000A) | DXN | Substantially Equivalent | |
| K904739 | DYNAPULSE 200M | DXN | 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