CKG 8800— 510(k) K823215
Substantially EquivalentCardio Kinetics, Inc.
FDA 510(k) clearance K823215 for CKG 8800, Substantially Equivalent on 1982-11-24. Applicant: Cardio Kinetics, Inc.. Device class: 2.
Clearance details
- Applicant
- Cardio Kinetics, Inc.
- Product code
- Code DSB
- Device class
- Class 2
- Regulation
- 21 CFR 870.2770
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code DSB
view allMore clearances from Cardio Kinetics, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.