RUSCH MANUAL RESUSCITATOR BAG— 510(k) K993194
Substantially EquivalentRusch, Inc.
FDA 510(k) clearance K993194 for RUSCH MANUAL RESUSCITATOR BAG, Substantially Equivalent on 2000-03-24. Applicant: Rusch, Inc.. Device class: 2.
Clearance details
- Applicant
- Rusch, Inc.
- Product code
- Code BTM
- Device class
- Class 2
- Regulation
- 21 CFR 868.5915
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Duluth, GA, US
Recent devices under product code BTM
view allMore clearances from Rusch, Inc.
view allAdverse events under product code BTM
product code BTM- Death
- 19
- Other
- 2
- Total
- 21
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.