ECHOCARDIOGRAPHY SYS., MODEL 3860— 510(k) K770756
Substantially EquivalentHoneywell, Inc.
FDA 510(k) clearance K770756 for ECHOCARDIOGRAPHY SYS., MODEL 3860, Substantially Equivalent on 1977-05-09. Applicant: Honeywell, Inc.. Device class: 2.
Clearance details
- Applicant
- Honeywell, Inc.
- Product code
- Code DXK
- Device class
- Class 2
- Regulation
- 21 CFR 870.2330
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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