VESSEL DILATOR
FDA 510(k) clearance K840641 · decided 1984-02-14
Clearance details
- K-number
- K840641
- Device name
- VESSEL DILATOR
- Applicant
- Aries Medical, Inc.
- Decision
- Unknown
- Date received
- 1984-02-14
- Decision date
- 1984-02-14
- Days to decision
- 0 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.