ROSSMAX AUTOMATIC WRISTWATCH BLOOD PRESSURE MONITOR, MODEL RM-4200— 510(k) K992388
Substantially EquivalentRossmax International , Ltd.
FDA 510(k) clearance K992388 for ROSSMAX AUTOMATIC WRISTWATCH BLOOD PRESSURE MONITOR, MODEL RM-4200, Substantially Equivalent on 1999-08-03. Applicant: Rossmax International , Ltd.. Device class: 2.
Clearance details
- Applicant
- Rossmax International , Ltd.
- Product code
- Product code DPW
- Device class
- Class 2
- Regulation
- 21 CFR 870.2100
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Taipei, TW
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Data sourced from openFDA. This site is unofficial and independent of the FDA.