I.V. START KIT, STERILE, DISPOSABLE— 510(k) K923361

Unknown

Trinity Laboratories, Inc.

FDA 510(k) clearance K923361 for I.V. START KIT, STERILE, DISPOSABLE, Unknown on 1993-06-28. Applicant: Trinity Laboratories, Inc.. Device class: 2.

Clearance details

Applicant
Trinity Laboratories, Inc.
Product code
Code LRS
Device class
Class 2
Regulation
21 CFR 880.5200
Advisory panel
General Hospital
Date received
Decision date
Decision
Unknown
Clearance type
Traditional
Location
Salisbury, MD, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code LRS

product code LRS
Other
2
Total
2

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.