DANNIFLEX MODEL 500TM CPM— 510(k) K904735
Substantially EquivalentBuckman Co., Inc.
FDA 510(k) clearance K904735 for DANNIFLEX MODEL 500TM CPM, Substantially Equivalent on 1991-01-30. Applicant: Buckman Co., Inc.. Device class: 1.
Clearance details
- Applicant
- Buckman Co., Inc.
- Product code
- Code BXB
- Device class
- Class 1
- Regulation
- 21 CFR 890.5380
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Concord, CA, US
Recent devices under product code BXB
view allMore clearances from Buckman Co., Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.