MICROPEAK— 510(k) K030586
Substantially EquivalentMicro Direct, Inc.
FDA 510(k) clearance K030586 for MICROPEAK, Substantially Equivalent on 2003-08-27. Applicant: Micro Direct, Inc.. Device class: 2.
Clearance details
- Applicant
- Micro Direct, Inc.
- Product code
- Code BZH
- Device class
- Class 2
- Regulation
- 21 CFR 868.1860
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Lewiston, ME, US
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