MODEL H39C-BEHING-THE-EAR HEARING INSTRU
FDA 510(k) clearance K790779 · decided 1979-05-16
Clearance details
- K-number
- K790779
- Device name
- MODEL H39C-BEHING-THE-EAR HEARING INSTRU
- Applicant
- Marcon Hearing Instruments, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1979-04-23
- Decision date
- 1979-05-16
- Days to decision
- 23 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.