DeviceClearance

MIC PEG TUBE— 510(k) K924065

Unknown

Medical Innovations Corp.

FDA 510(k) clearance K924065 for MIC PEG TUBE, Unknown on 1994-02-17. Applicant: Medical Innovations Corp.. Device class: 2.

Clearance details

Applicant
Medical Innovations Corp.
Product code
Code KNT
Device class
Class 2
Regulation
21 CFR 876.5980
Advisory panel
Gastroenterology, Urology
Date received
Decision date
Decision
Unknown
Clearance type
Traditional
Location
Milpitas, CA, US
Download summary PDFView on FDA.gov ↗

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More clearances from Medical Innovations Corp.

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Adverse events under product code KNT

product code KNT
Death
192
Injury
6,034
Malfunction
4,049
Other
1
Total
10,276

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 K924065

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 K924065.

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