MODIFIED ESCHMANN DILATATION CATHETER
FDA 510(k) clearance K864637 · decided 1987-01-06
Clearance details
- K-number
- K864637
- Device name
- MODIFIED ESCHMANN DILATATION CATHETER
- Applicant
- Eschmann Bros. & Walsh , Ltd.
- Decision
- Substantially Equivalent
- Date received
- 1986-11-19
- Decision date
- 1987-01-06
- Days to decision
- 48 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Sussex Bn15 8tj, GB
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.