SPACELABS MULTI-PARAMETER MODULE— 510(k) K103142

Substantially Equivalent

Spacelabs Healthcare, Inc.

FDA 510(k) clearance K103142 for SPACELABS MULTI-PARAMETER MODULE, Substantially Equivalent on 2011-03-03. Applicant: Spacelabs Healthcare, Inc.. Device class: 2.

Clearance details

Applicant
Spacelabs Healthcare, Inc.
Product code
Code DSI
Device class
Class 2
Regulation
21 CFR 870.1025
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Nederland, CO, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code DSI

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Adverse events under product code DSI

product code DSI
Death
170
Injury
729
Malfunction
10,680
Total
11,579

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recalls naming K103142

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K103142.

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