CUFF PACER— 510(k) K780703
Substantially EquivalentOmp Laboratories, Inc.
FDA 510(k) clearance K780703 for CUFF PACER, Substantially Equivalent on 1978-07-17. Applicant: Omp Laboratories, Inc.. Device class: 2.
Clearance details
- Applicant
- Omp Laboratories, Inc.
- Product code
- Code CBA
- Device class
- Class 2
- Regulation
- 21 CFR 868.2025
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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