FLOCARE— 510(k) K893875
Substantially EquivalentMega-Tech Intl., Inc.
FDA 510(k) clearance K893875 for FLOCARE, Substantially Equivalent on 1989-08-11. Applicant: Mega-Tech Intl., Inc.. Device class: 1.
Clearance details
- Applicant
- Mega-Tech Intl., Inc.
- Product code
- Code BYD
- Device class
- Class 1
- Regulation
- 21 CFR 868.5375
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wayne, PA, US
Recent devices under product code BYD
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