ASPIRATION NEEDLE
FDA 510(k) clearance K780784 · decided 1978-08-14
Clearance details
- K-number
- K780784
- Device name
- ASPIRATION NEEDLE
- Applicant
- Ferris Mfg. Corp.
- Decision
- Substantially Equivalent
- Date received
- 1978-05-12
- Decision date
- 1978-08-14
- Days to decision
- 94 days
- Clearance type
- Traditional
- Product code
- KKX
- Device class
- 2
- Regulation number
- 878.4370
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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| 3M STERI-DRAPE FABRIC SURGICAL DRAPES (K140330) | 3M Healthcare | 2014-08-18 |
| WHITNEY MEDICAL SOLUTIONS ESHIELD (K141438) | Whitney Medical Solutions | 2014-08-14 |
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Recalls involving this device
No recalls on record reference this clearance.