MICROFLATOR— 510(k) K771679
Substantially EquivalentFisons Corp.
FDA 510(k) clearance K771679 for MICROFLATOR, Substantially Equivalent on 1977-09-28. Applicant: Fisons Corp.. Device class: 1.
Clearance details
- Applicant
- Fisons Corp.
- Product code
- Code FLG
- Device class
- Class 1
- Regulation
- 21 CFR 880.6150
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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