NON STERILE PARENTERAL SUPPLY KIT— 510(k) K900857

Unknown

Intermed, Inc.

FDA 510(k) clearance K900857 for NON STERILE PARENTERAL SUPPLY KIT, Unknown on 1990-05-22. Applicant: Intermed, Inc..

Clearance details

Applicant: Intermed, Inc.
Product code: Code FMF
Advisory panel: General Hospital
Date received: 1990-02-23
Decision date: 1990-05-22
Decision: Unknown
Clearance type: Traditional
Location: Sparta, NJ, US

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Adverse events under product code FMF

product code FMF

Death: 15
Injury: 2,263
Malfunction: 29,722
Other: 17
Total: 32,017

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. 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.