DeviceClearance

PATIENT MONITOR CM111, 112— 510(k) K810178

Substantially Equivalent

Honeywell, Inc.

FDA 510(k) clearance K810178 for PATIENT MONITOR CM111, 112, 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
Download summary PDFView on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.