MEDSURG SELDINGER NEEDLE
FDA 510(k) clearance K854294 · decided 1986-01-13
Clearance details
- K-number
- K854294
- Device name
- MEDSURG SELDINGER NEEDLE
- Applicant
- Medsurg Industries, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1985-10-25
- Decision date
- 1986-01-13
- Days to decision
- 80 days
- Clearance type
- Traditional
- Product code
- DRC
- Device class
- 2
- Regulation number
- 870.1390
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Herndon, VA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.