PATIENT CARE MANAGEMENT SYSTEM MODIFICATION— 510(k) K910029

Substantially Equivalent

Spacelabs, Inc.

FDA 510(k) clearance K910029 for PATIENT CARE MANAGEMENT SYSTEM MODIFICATION, Substantially Equivalent on 1991-01-31. Applicant: Spacelabs, Inc.. Device class: 2.

Clearance details

Applicant
Spacelabs, 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
Redmond, WA, US
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