PASSPORT V MONITOR, MODEL 0998-00-6100— 510(k) K091834
Substantially EquivalentDatascope Corp., Patient Monitoring Division
FDA 510(k) clearance K091834 for PASSPORT V MONITOR, MODEL 0998-00-6100, Substantially Equivalent on 2009-07-15. Applicant: Datascope Corp., Patient Monitoring Division. Device class: 2.
Clearance details
- Applicant
- Datascope Corp., Patient Monitoring Division
- Product code
- Code MHX
- Device class
- Class 2
- Regulation
- 21 CFR 870.1025
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Mahwh, NJ, US
Recent devices under product code MHX
view allMore clearances from Datascope Corp., Patient Monitoring Division
view allAdverse events under product code MHX
product code MHX- Death
- 580
- Injury
- 2,441
- Malfunction
- 12,655
- Other
- 3
- Total
- 15,679
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 →
Recalls naming K091834
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K091834.
Data sourced from openFDA. This site is unofficial and independent of the FDA.