Procedure Products, Inc.
FDA 510(k) & PMA Approved Devices — 16 products
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Total Devices16
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K161812 | Freedom Syringe | FMF | 2017-03-27 | View |
| 510(k) | K923194 | INSUFFLATOR CONNECTING FILTER | HIF | 1993-10-08 | View |
| 510(k) | K922536 | TORQUE DEVICE | DQX | 1992-12-10 | View |
| 510(k) | K914128 | CONNECTING SET | DQO | 1991-11-27 | View |
| 510(k) | K910673 | BAG SPIGOT | KPE | 1991-04-24 | View |
| 510(k) | K884985 | MODIFIED 10CC SYRINGE CONTROL RING SET | FMF | 1988-12-20 | View |
| 510(k) | K874747 | 10CC SYRINGE CONTROL RING SET | FMF | 1988-02-04 | View |
| 510(k) | K874037 | ANGIO WASTE FLUIDS DUMP BAG | DQO | 1988-01-29 | View |
| 510(k) | K853749 | CUSTOM CORONARY MANIFOLD KITS | DTL | 1986-01-13 | View |
| 510(k) | K842173 | DISPOSABLE STOPCOCKS | FMG | 1984-09-05 | View |
| 510(k) | K833554 | MATERIAL ADDITION LEXAN & K-RESIN | DQO | 1984-03-12 | View |
| 510(k) | K820384 | GLASS SYRINGES, DRUG, LUER LOCK | FMF | 1982-04-15 | View |
| 510(k) | K812657 | INJECTION CAP, LUER LOCK | FPA | 1981-10-23 | View |
| 510(k) | K811548 | CERVICAL SPATULA | HHT | 1981-06-23 | View |
| 510(k) | K810921 | MALE LUER LOCK PLUGS | FPA | 1981-05-21 | View |
| 510(k) | K810859 | SINGLE USE SELDINGER/COURNAND PERC. NDL | DRE | 1981-04-11 | View |
No matching devices.
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