RADIOEAR MODEL 1072
FDA 510(k) clearance K770402 · decided 1977-03-10
Clearance details
- K-number
- K770402
- Device name
- RADIOEAR MODEL 1072
- Applicant
- Radioear Corp.
- Decision
- Substantially Equivalent
- Date received
- 1977-03-03
- Decision date
- 1977-03-10
- Days to decision
- 7 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.