SIMPLICITY SERIES 5— 510(k) K881634
Substantially EquivalentQuartet Technology, Inc.
FDA 510(k) clearance K881634 for SIMPLICITY SERIES 5, Substantially Equivalent on 1988-05-17. Applicant: Quartet Technology, Inc.. Device class: 2.
Clearance details
- Applicant
- Quartet Technology, Inc.
- Product code
- Code IQA
- Device class
- Class 2
- Regulation
- 21 CFR 890.3725
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tyngsboro, MA, US
Recent devices under product code IQA
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