MAGLINTE ENTEROCLYSIS CATHETER— 510(k) K884379
Substantially EquivalentLafayette Pharmacal, Inc.
FDA 510(k) clearance K884379 for MAGLINTE ENTEROCLYSIS CATHETER, Substantially Equivalent on 1989-02-28. Applicant: Lafayette Pharmacal, Inc.. Device class: 2.
Clearance details
- Applicant
- Lafayette Pharmacal, Inc.
- Product code
- Code FGD
- Device class
- Class 2
- Regulation
- 21 CFR 876.5980
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Lafayette, IN, US
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