MARTIN PELVIC LIFT— 510(k) K823206
Substantially EquivalentMartin Pelvic Lift Co.
FDA 510(k) clearance K823206 for MARTIN PELVIC LIFT, Substantially Equivalent on 1983-04-28. Applicant: Martin Pelvic Lift Co.. Device class: 1.
Clearance details
- Applicant
- Martin Pelvic Lift Co.
- Product code
- Code FSA
- Device class
- Class 1
- Regulation
- 21 CFR 880.5510
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code FSA
view allAdverse events under product code FSA
product code FSA- Death
- 101
- Injury
- 767
- Malfunction
- 1,173
- Other
- 1
- Total
- 2,042
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.