DeviceClearance

ECHOCARDIOGRAPHY SYS., MODEL 3830— 510(k) K770755

Substantially Equivalent

Honeywell, Inc.

FDA 510(k) clearance K770755 for ECHOCARDIOGRAPHY SYS., MODEL 3830, Substantially Equivalent on 1977-05-09. Applicant: Honeywell, Inc..

Clearance details

Applicant
Honeywell, Inc.
Product code
Code DXK
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Mchenry, IL, US
Download summary PDFView on FDA.gov ↗

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