VITALMAX 530— 510(k) K932203
Substantially EquivalentPace Tech Medical Monitors, Inc.
FDA 510(k) clearance K932203 for VITALMAX 530, Substantially Equivalent on 1994-07-19. Applicant: Pace Tech Medical Monitors, Inc.. Device class: 2.
Clearance details
- Applicant
- Pace Tech Medical Monitors, Inc.
- Product code
- Code DQA
- Device class
- Class 2
- Regulation
- 21 CFR 870.2700
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Clearwater, FL, US
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More clearances from Pace Tech Medical Monitors, Inc.
view allAdverse events under product code DQA
product code DQA- Death
- 66
- Malfunction
- 2,867
- Other
- 1
- Total
- 2,934
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.