MYOLEX— 510(k) K863730
Substantially EquivalentOrion Corp.
FDA 510(k) clearance K863730 for MYOLEX, Substantially Equivalent on 1986-10-15. Applicant: Orion Corp.. Device class: 2.
Clearance details
- Applicant
- Orion Corp.
- Product code
- Code DDR
- Device class
- Class 2
- Regulation
- 21 CFR 866.5680
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- 20101 Turku, FI
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More clearances from Orion Corp.
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