CARDIOPHONICS 1000 MEMORY MONITOR— 510(k) K992772
Substantially EquivalentRlt Medical Assoc., Inc.
FDA 510(k) clearance K992772 for CARDIOPHONICS 1000 MEMORY MONITOR, Substantially Equivalent on 1999-09-17. Applicant: Rlt Medical Assoc., Inc.. Device class: 2.
Clearance details
- Applicant
- Rlt Medical Assoc., Inc.
- Product code
- Code DXH
- Device class
- Class 2
- Regulation
- 21 CFR 870.2920
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Timonium, MD, US
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