DEFIBRILLATOR ANALYZER MODEL QED-5— 510(k) K904159
Substantially EquivalentBio-Tek Instruments, Inc.
FDA 510(k) clearance K904159 for DEFIBRILLATOR ANALYZER MODEL QED-5, Substantially Equivalent on 1991-03-18. Applicant: Bio-Tek Instruments, Inc..
Clearance details
- Applicant
- Bio-Tek Instruments, Inc.
- Product code
- Code DRL
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Winooski, VT, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.