PACEMAKER PATIENT ADAPTOR MODULE (PPAM)— 510(k) K900213
Substantially EquivalentBomed Medical Mfg., Ltd.
FDA 510(k) clearance K900213 for PACEMAKER PATIENT ADAPTOR MODULE (PPAM), Substantially Equivalent on 1990-06-28. Applicant: Bomed Medical Mfg., Ltd.. Device class: 2.
Clearance details
- Applicant
- Bomed Medical Mfg., Ltd.
- Product code
- Code DSB
- Device class
- Class 2
- Regulation
- 21 CFR 870.2770
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Irvine, CA, US
Recent devices under product code DSB
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