Promedic, Inc.
Promedic, Inc. holds FDA 510(k) medical device clearances, first cleared 1995, most recent 2014.
Top product codes for Promedic, Inc.
Recent clearances by Promedic, Inc.
- K131889 — EUM 100PRO
- K112318 — CLEARPATH 24
- K072756 — NON-IV ADAPTER FOR INFANT NG TUBE
- K060497 — BABYAIR
- K060842 — REVJET TURBO
- K052903 — PEDIATRIC FEEDING TUBE
- K031409 — URINARY CATHETERS
- K024190 — FENESTRATED INFUSION CATHETER
- K023579 — GAS SAMPLING LINES
- K020005 — INFANT FEEDING TUBES
- K970102 — FILTER
- K970991 — DATEX ENGSTOM MANUAL RESUSCITATOR
- K962182 — BURLEW INFANT HOOD
- K954201 — BUONAFEDE PNEUMATIC SLEEVE
- K951988 — PRESSURIZER
- K951043 — AIR-SOFT-DISPOSABLE, ANESTHESISA/RESPIRATORY FACE MASK
Data sourced from openFDA. This site is unofficial and independent of the FDA.