Feliks Plastik Laminasyon VE Ambalaj Malzemeleri is one of 37 FDA 510(k) medical device manufacturers from Turkey in the dataset, ranked by real submission volume.
Feliks Plastik Laminasyon VE Ambalaj Malzemeleri - FDA 510(k) Cleared...
Recent clearances: Bodygard SFS Surgical Gown Level 4
1
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Cleared
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Denied
Feliks Plastik Laminasyon VE Ambalaj Malzemeleri has 1 FDA 510(k) cleared medical devices. Based in Odunpazari, TR.
Last cleared in 2022. Active since 2022. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Feliks Plastik Laminasyon VE Ambalaj Malzemeleri Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Dp Distribution & Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Feliks Plastik Laminasyon VE Ambalaj Malzemeleri
1 devices