L-3 PURGE LINE— 510(k) K802602
Substantially EquivalentDelta Medical Industries
FDA 510(k) clearance K802602 for L-3 PURGE LINE, Substantially Equivalent on 1980-11-12. Applicant: Delta Medical Industries. Device class: 2.
Clearance details
- Applicant
- Delta Medical Industries
- Product code
- Code DTM
- Device class
- Class 2
- Regulation
- 21 CFR 870.4260
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code DTM
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