DTC
Hangzhou DTC Medical Apparatus Co., Ltd. · Model 0.018/0.022 · UDI-DI 06973554430491
2
510(k) clearances
5
Adverse events
1
Recalls
85
Facilities
Description
Ceremic brackets
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-11-13 | Karl Storz Endoscopy America Inc | KARL STORZ Endoscopy America, Inc. is recalling the Flexible Broncho Fiberscope or a Flexible Intubation Fiberscope with a suction port because the material used in the suction cha |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.