ADAPTER KIT— 510(k) K800353
Substantially EquivalentDaig Corp.
FDA 510(k) clearance K800353 for ADAPTER KIT, Substantially Equivalent on 1980-05-28. Applicant: Daig Corp.. Device class: 2.
Clearance details
- Applicant
- Daig Corp.
- Product code
- Code DTD
- Device class
- Class 2
- Regulation
- 21 CFR 870.3620
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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