VENES CUSTON RX— 510(k) K820484
Substantially EquivalentJung Products, Inc.
FDA 510(k) clearance K820484 for VENES CUSTON RX, Substantially Equivalent on 1982-03-18. Applicant: Jung Products, Inc.. Device class: 1.
Clearance details
- Applicant
- Jung Products, Inc.
- Product code
- Code FQL
- Device class
- Class 1
- Regulation
- 21 CFR 880.5780
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code FQL
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view allAdverse events under product code FQL
product code FQL- Other
- 1
- Total
- 1
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.