HUMIDI-FLEX TM— 510(k) K885313
Substantially EquivalentLife Design Systems, Inc.
FDA 510(k) clearance K885313 for HUMIDI-FLEX TM, Substantially Equivalent on 1989-10-11. Applicant: Life Design Systems, Inc.. Device class: 1.
Clearance details
- Applicant
- Life Design Systems, Inc.
- Product code
- Code BYD
- Device class
- Class 1
- Regulation
- 21 CFR 868.5375
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Franklin, WI, US
Recent devices under product code BYD
view allMore clearances from Life Design Systems, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.