Richard-Allan Medical
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K942207 | REFLEX INS INSUFFLATION NEEDLE | HIF | 1994-05-27 | View |
| 510(k) | K935105 | REFLEX ESP WITH FINGER SWITCHES | GEI | 1994-02-22 | View |
| 510(k) | K933508 | REFLEX SDD SURGICAL STAPLER | GEF | 1993-11-23 | View |
| 510(k) | K933901 | REFLEX(R) EHS (ENDOSCOPIC HERNIA STAPLER) | GAG | 1993-11-19 | View |
| 510(k) | K924881 | REFLEX(R) ESP | GEI | 1993-07-23 | View |
| 510(k) | K924929 | REFLEX(R) ECA | HBT | 1993-07-21 | View |
| 510(k) | K905701 | RICHARD-ALLAN SHEET CLIP | KKX | 1991-02-19 | View |
| 510(k) | K905682 | RICHARD-ALLAN CLAMP COVERS | FSM | 1991-02-19 | View |
No matching devices.
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