KOPANS HOOKWIRE LESION LOCALIZATION NEEDLE— 510(k) K900903
Substantially EquivalentMilex Products, Inc.
FDA 510(k) clearance K900903 for KOPANS HOOKWIRE LESION LOCALIZATION NEEDLE, Substantially Equivalent on 1990-05-03. Applicant: Milex Products, Inc.. Device class: 1.
Clearance details
- Applicant
- Milex Products, Inc.
- Product code
- Code GDF
- Device class
- Class 1
- Regulation
- 21 CFR 878.4800
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Chicago, IL, US
Recent devices under product code GDF
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