K790779Substantially Equivalent
Model H39c-Behing-the-Ear Hearing Instru
Marcon Hearing Instruments, Inc., Mchenry IL / Traditional, Substantially Equivalent
K790779 is the FDA 510(k) clearance record for MODEL H39C-BEHING-THE-EAR HEARING INSTRU, cleared for Marcon Hearing Instruments, Inc. on . FDA records list 10 510(k) clearances for Marcon Hearing Instruments, Inc., from to . As of , FDA records show no recalls naming K790779.
Clearance record
- Decision date
- Received
- (23 days to decision)
- Review panel
- Unknown
- Applicant
- Marcon Hearing Instruments, Inc. 803 N. Front St. Suite 3, Mchenry IL
- Third party review
- No
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
