DeviceClearance

CADD -SOLIS AMBULATORY INFUSION PUMP AND CADD -SOLIS MEDICATION SAFETY SOFTWARE - ADMINISTRATOR— 510(k) K072144

Substantially Equivalent

Smiths Medical MD, Inc.

FDA 510(k) clearance K072144 for CADD -SOLIS AMBULATORY INFUSION PUMP AND CADD -SOLIS MEDICATION SAFETY SOFTWARE - ADMINISTRATOR, Substantially Equivalent on 2008-03-07. Applicant: Smiths Medical MD, Inc.. Device class: 2.

Clearance details

Applicant
Smiths Medical MD, Inc.
Product code
Code MEA
Device class
Class 2
Regulation
21 CFR 880.5725
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
St. Paul, MN, US
Download summary PDFView on FDA.gov ↗

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More clearances from Smiths Medical MD, Inc.

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Adverse events under product code MEA

product code MEA
Death
19
Malfunction
25,089
Total
25,108

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 K072144

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 K072144.

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