OMNIMEDICAL QUAD II DIGITAL ANGIOGRAPH SYSTEM
FDA 510(k) clearance K837378 · decided 1983-05-18
Clearance details
- K-number
- K837378
- Device name
- OMNIMEDICAL QUAD II DIGITAL ANGIOGRAPH SYSTEM
- Applicant
- Omnimedical
- Decision
- Substantially Equivalent
- Date received
- 1983-03-17
- Decision date
- 1983-05-18
- Days to decision
- 62 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.