510(k) K983832
K983832 is an FDA 510(k) premarket notification submitted by Idem (Int'L Dist. of Electronics For Medicine) for the device "INTERACOUSTICS MODEL MT 10, HANDHELD IMPEDANCE AUDIOMETER". The FDA issued a decision of Substantially Equivalent on January 25, 1999. The device falls under product code ETY (Tester, Auditory Impedance), a Class II device regulated under 21 CFR 874.1090. Idem (Int'L Dist. of Electronics For Medicine) has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 25, 1999
- Date Received
- October 30, 1998
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Tester, Auditory Impedance
- Device Class
- Class II
- Regulation Number
- 874.1090
- Review Panel
- EN
- Submission Type