AMPLAID MARK 4 AND MARK 5— 510(k) K781667
Substantially EquivalentAmplaid USA, Inc.
FDA 510(k) clearance K781667 for AMPLAID MARK 4 AND MARK 5, Substantially Equivalent on 1978-11-03. Applicant: Amplaid USA, Inc.. Device class: 2.
Clearance details
- Applicant
- Amplaid USA, Inc.
- Product code
- Code GWJ
- Device class
- Class 2
- Regulation
- 21 CFR 882.1900
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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