0.9% SODIUM CHLORIDE FLISH SYRINGE
FDA 510(k) clearance K120836 · decided 2012-07-12
Clearance details
- K-number
- K120836
- Device name
- 0.9% SODIUM CHLORIDE FLISH SYRINGE
- Applicant
- Am USA
- Decision
- Substantially Equivalent
- Date received
- 2012-03-20
- Decision date
- 2012-07-12
- Days to decision
- 114 days
- Clearance type
- Special
- Product code
- NGT
- Device class
- 2
- Regulation number
- 880.5200
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Nashville, TN, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
| Record | Firm | Date |
|---|---|---|
| 0.9% Sodium Chloride Injection, USP, 10mL in 12mL., Single use, Rx only, Sterile Solution. recall (Z-2476-2015) | MRP, LLC dba AMUSA | 2015-08-27 |
| T/S2 0.9% Sodium Chloride Injection, USP, AMUSA Sterile Field Flush Syringe, 10 mL in 12 m recall (Z-1808-2015) | MRP, LLC dba AMUSA | 2015-06-15 |