THE INHIBITOR, MODEL 001— 510(k) K070648
Substantially EquivalentMelmedtronics, Inc.
FDA 510(k) clearance K070648 for THE INHIBITOR, MODEL 001, Substantially Equivalent on 2007-06-29. Applicant: Melmedtronics, Inc.. Device class: 2.
Clearance details
- Applicant
- Melmedtronics, Inc.
- Product code
- Code KLW
- Device class
- Class 2
- Regulation
- 21 CFR 874.3400
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hurst, TX, US
Recent devices under product code KLW
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