30-30-2 700 SYRINGE EXTENSION SET
FDA 510(k) clearance K811885 · decided 1981-08-25
Clearance details
- K-number
- K811885
- Device name
- 30-30-2 700 SYRINGE EXTENSION SET
- Applicant
- Y
- Decision
- Substantially Equivalent
- Date received
- 1981-07-01
- Decision date
- 1981-08-25
- Days to decision
- 55 days
- Clearance type
- Traditional
- Product code
- FPA
- Device class
- 2
- Regulation number
- 880.5440
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Y
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
Recalls involving this device
| Record | Firm | Date |
|---|---|---|
| SmartSite Syringe Administration Set-Product Package Size 50, Catalog Number: 10798696 recall (Z-1210-2019) | Becton Dickinson & Company | 2019-06-26 |