DUAL TRACE PATIENT MONITOR 116,118,120— 510(k) K810179
Substantially EquivalentHoneywell, Inc.
FDA 510(k) clearance K810179 for DUAL TRACE PATIENT MONITOR 116,118,120, Substantially Equivalent on 1981-02-25. Applicant: Honeywell, Inc..
Clearance details
- Applicant
- Honeywell, Inc.
- Product code
- Code DSK
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.