INSULSCAN INSULATION TESTING SYSTEM
FDA 510(k) clearance K991424 · decided 1999-07-22
Clearance details
- K-number
- K991424
- Device name
- INSULSCAN INSULATION TESTING SYSTEM
- Applicant
- Medicor Corp.
- Decision
- Substantially Equivalent
- Date received
- 1999-04-23
- Decision date
- 1999-07-22
- Days to decision
- 90 days
- Clearance type
- Traditional
- Product code
- HFG
- Device class
- 2
- Regulation number
- 884.4160
- Medical specialty
- Obstetrics/Gynecology
- Advisory committee
- Obstetrics/Gynecology
- Location
- Vernon Hills, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.