NEOMED ENTERAL ONLY EXTENSION SET— 510(k) K100288
Substantially EquivalentNeomed, Inc.
FDA 510(k) clearance K100288 for NEOMED ENTERAL ONLY EXTENSION SET, Substantially Equivalent on 2010-08-03. Applicant: Neomed, Inc.. Device class: 2.
Clearance details
- Applicant
- Neomed, Inc.
- Product code
- Code KNT
- Device class
- Class 2
- Regulation
- 21 CFR 876.5980
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Swanee, GA, US
Recent devices under product code KNT
view allMore clearances from Neomed, Inc.
view all- K183540 — Oral/Enteral Syringes with ENFit connector (12 mL to 60 mL), Low Dose Tip Oral/Enteral Syringes with ENFit connector (1 mL to 6 mL)
- K161039 — NeoConnect Oral/Enteral Syringes with ENFit connector (12 mL to 100 mL) and NeoConnect Low Dose Tip Oral/Enteral Syringes with ENFit connector (0.5 mL to 6mL)
- K152857 — NeoMed NeoConnect Enteral Syringes with ENFit Connector and compatible NeoSecure Tip Caps
- K143344 — NeoMed NeoConnect Enteral Syringes with ENFit Connector
- K122373 — NEOMED ORAL/ENTERAL SYRINGE
Adverse events under product code KNT
product code KNT- Death
- 192
- Injury
- 6,034
- Malfunction
- 4,049
- Other
- 1
- Total
- 10,276
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recalls naming K100288
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K100288.
Data sourced from openFDA. This site is unofficial and independent of the FDA.