CANNULA, IV
FDA 510(k) clearance K760389 · decided 1976-11-02
Clearance details
- K-number
- K760389
- Device name
- CANNULA, IV
- Applicant
- B. Braun Instruments
- Decision
- Substantially Equivalent
- Date received
- 1976-08-05
- Decision date
- 1976-11-02
- Days to decision
- 89 days
- Clearance type
- Traditional
- Product code
- FGY
- Device class
- 1
- Regulation number
- 878.4200
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch B. Braun Instruments
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.
| Record | Firm | Date |
|---|---|---|
| EAR CANNULAS (K822201) | Kelleher Corp. | 1982-10-06 |
Recalls involving this device
No recalls on record reference this clearance.