SURGI-TEK TUBE POSITIONER
FDA 510(k) clearance K863279 · decided 1986-09-09
Clearance details
- K-number
- K863279
- Device name
- SURGI-TEK TUBE POSITIONER
- Applicant
- Dermacare Products, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1986-08-25
- Decision date
- 1986-09-09
- Days to decision
- 15 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Louisville, KT, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.