INTRALIG— 510(k) K823536
Substantially EquivalentMiltex Instrument Co.
FDA 510(k) clearance K823536 for INTRALIG, Substantially Equivalent on 1982-12-28. Applicant: Miltex Instrument Co.. Device class: 2.
Clearance details
- Applicant
- Miltex Instrument Co.
- Product code
- Code EJI
- Device class
- Class 2
- Regulation
- 21 CFR 872.6770
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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