MICROGUIDE LESION MARKING SYSTEM— 510(k) K923120
Substantially EquivalentAngiodynamics, Div. E-Z-Em, Inc.
FDA 510(k) clearance K923120 for MICROGUIDE LESION MARKING SYSTEM, Substantially Equivalent on 1992-09-01. Applicant: Angiodynamics, Div. E-Z-Em, Inc.. Device class: 1.
Clearance details
- Applicant
- Angiodynamics, Div. E-Z-Em, 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
- Glens Falls, NY, US
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