CAMINO VENTRICULAR NEEDLE
FDA 510(k) clearance K920088 · decided 1992-05-01
Clearance details
- K-number
- K920088
- Device name
- CAMINO VENTRICULAR NEEDLE
- Applicant
- Camino Laboratories, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1992-01-08
- Decision date
- 1992-05-01
- Days to decision
- 114 days
- Clearance type
- Traditional
- Product code
- HCD
- Device class
- 1
- Regulation number
- 882.4060
- Medical specialty
- Neurology
- Advisory committee
- Neurology
- Location
- San Diego, CA, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| Alcyone MEMS Cannula (AMC) System (K150660) | Alcyone Lifesciences, Inc. | 2015-04-16 |
| SURGIVISION MR COMPATIBLE VENTRICULAR CANNULA (K102101) | Surgivision, Inc. | 2011-01-26 |
Recalls involving this device
No recalls on record reference this clearance.