NEEDLE GUIDE MODEL 21285A
FDA 510(k) clearance K830753 · decided 1983-06-16
Clearance details
- K-number
- K830753
- Device name
- NEEDLE GUIDE MODEL 21285A
- Applicant
- Hewlett-Packard Co.
- Decision
- Substantially Equivalent
- Date received
- 1983-03-10
- Decision date
- 1983-06-16
- Days to decision
- 98 days
- Clearance type
- Traditional
- Product code
- LFL
- Device class
- U
- Medical specialty
- Unknown
- Advisory committee
- Unknown
- Location
- Walker, MI, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
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Recalls involving this device
No recalls on record reference this clearance.