SURESET 3.0 ML RESERVOIR, MODEL 24-103— 510(k) K024056

Substantially Equivalent

Applied Diabetes Research, Incorporated

FDA 510(k) clearance K024056 for SURESET 3.0 ML RESERVOIR, MODEL 24-103, Substantially Equivalent on 2003-01-17. Applicant: Applied Diabetes Research, Incorporated. Device class: 2.

Clearance details

Applicant
Applied Diabetes Research, Incorporated
Product code
Code FRN
Device class
Class 2
Regulation
21 CFR 880.5725
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Laguna Niguel, CA, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code FRN

product code FRN
Death
540
Injury
6,178
Malfunction
1,464,165
Other
52
Total
1,470,935

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 →

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