Home › Device types › OAY
Light Source System, Diagnostic Endoscopic
FDA product code OAY · Class 3 · Unknown
16
Registered devices
12
Adverse events
1
Recalls
0
510(k) clearances
Devices with this code
NA — Karl Storz GmbH & Co. KGTRICAM® — Karl Storz GmbH & Co. KGTRICAM® — Karl Storz GmbH & Co. KGn.a. — Karl Storz GmbH & Co. KGTRICAM® — Karl Storz GmbH & Co. KGHOPKINS — Karl Storz GmbH & Co. KGD-LIGHT C — Karl Storz GmbH & Co. KGn.a. — Karl Storz GmbH & Co. KGn.a. — Karl Storz GmbH & Co. KGHOPKINS — Karl Storz GmbH & Co. KGn.a. — Karl Storz GmbH & Co. KGHOPKINS — Karl Storz GmbH & Co. KGn.a. — Karl Storz GmbH & Co. KGNA — Karl Storz GmbH & Co. KGHOPKINS — Karl Storz GmbH & Co. KGTRICAM® — Karl Storz GmbH & Co. KG
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2012-08-16 | Karl Storz Endoscopy America Inc | The recall was initiated because Karl Storz has confirmed that the Photodynamic Diagnosis (PDD) D-Light C System instruction manuals have important safety-relat |
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