GERONIMO— 510(k) K935750
Substantially Equivalent for Some IndicationsRedman, Inc.
FDA 510(k) clearance K935750 for GERONIMO, Substantially Equivalent for Some Indications on 1995-02-03. Applicant: Redman, Inc.. Device class: 2.
Clearance details
- Applicant
- Redman, Inc.
- Product code
- Code ITI
- Device class
- Class 2
- Regulation
- 21 CFR 890.3860
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent for Some Indications
- Clearance type
- Traditional
- Location
- Tucson, AZ, US
Recent devices under product code ITI
view allMore clearances from Redman, Inc.
view allAdverse events under product code ITI
product code ITI- Death
- 34
- Injury
- 778
- Malfunction
- 1,085
- Other
- 1
- Total
- 1,898
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.