DeviceClearance

VIAL2BAG— 510(k) K072759

Substantially Equivalent

Medimop Medical Projects, Ltd.

FDA 510(k) clearance K072759 for VIAL2BAG, Substantially Equivalent on 2007-12-13. Applicant: Medimop Medical Projects, Ltd.. Device class: 2.

Clearance details

Applicant
Medimop Medical Projects, Ltd.
Product code
Code LHI
Device class
Class 2
Regulation
21 CFR 880.5440
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Abbreviated
Location
Lionville, PA, US
Download summary PDFView on FDA.gov ↗

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More clearances from Medimop Medical Projects, Ltd.

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Adverse events under product code LHI

product code LHI
Injury
207
Malfunction
7,820
Other
3
Total
8,030

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 K072759

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 K072759.

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