ARBO H79P DISPOSABLE MONITORING ELECTRODES— 510(k) K894562
Substantially EquivalentArbo Medical, Inc.
FDA 510(k) clearance K894562 for ARBO H79P DISPOSABLE MONITORING ELECTRODES, Substantially Equivalent on 1989-09-05. Applicant: Arbo Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Arbo Medical, Inc.
- Product code
- Code DRX
- Device class
- Class 2
- Regulation
- 21 CFR 870.2360
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wilton, CT, US
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Adverse events under product code DRX
product code DRX- Death
- 6
- Injury
- 476
- Other
- 2
- Total
- 484
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.