MAXI-FLOW— 510(k) K955150
Substantially EquivalentBio-Medical Devices, Inc.
FDA 510(k) clearance K955150 for MAXI-FLOW, Substantially Equivalent on 1996-01-23. Applicant: Bio-Medical Devices, Inc.. Device class: 2.
Clearance details
- Applicant
- Bio-Medical Devices, Inc.
- Product code
- Code BYY
- Device class
- Class 2
- Regulation
- 21 CFR 880.6740
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Irvine, CA, US
Recent devices under product code BYY
view allMore clearances from Bio-Medical Devices, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.