AMPLITONE-3— 510(k) K812676
Substantially EquivalentProgressive Technology, Inc.
FDA 510(k) clearance K812676 for AMPLITONE-3, Substantially Equivalent on 1981-10-13. Applicant: Progressive Technology, Inc.. Device class: 1.
Clearance details
- Applicant
- Progressive Technology, Inc.
- Product code
- Code LDE
- Device class
- Class 1
- Regulation
- 21 CFR 870.1875
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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