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Marina Medical
MARINA MEDICAL INSTRUMENTS, INC. · Model 042-048 · UDI-DI 00840306836152
10
510(k) clearances
49
Adverse events
1
Recalls
719
Facilities
Description
Bowman Lacrimal Duct Probe, 1.7/1.8mm, 7-8
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2008-06-05 | Phillips Safety Products | Radiation Protective Eyewear does not meet the radiation protection levels stated on the labeling. |
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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.