THE SUTURER
FDA 510(k) clearance K842912 · decided 1984-08-15
Clearance details
- K-number
- K842912
- Device name
- THE SUTURER
- Applicant
- Vlm Surgical, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1984-07-25
- Decision date
- 1984-08-15
- Days to decision
- 21 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Walker, MI, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.