AUTOMATIC EXPOSURE CONTROL TYPE A3300
FDA 510(k) clearance K827525 · decided 1982-06-18
Clearance details
- K-number
- K827525
- Device name
- AUTOMATIC EXPOSURE CONTROL TYPE A3300
- Applicant
- Advanced Instrument Development, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1982-05-21
- Decision date
- 1982-06-18
- Days to decision
- 28 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Melrose Park, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.