510(k) K895815
K895815 is an FDA 510(k) premarket notification submitted by Microbio-Medics, Inc. for the device "MICROTEK TOTAL OSSICULAR PROTHESIS". The FDA issued a decision of Substantially Equivalent on December 26, 1989. The device falls under product code ETA (Replacement, Ossicular Prosthesis, Total), a Class II device regulated under 21 CFR 874.3495. Microbio-Medics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 26, 1989
- Date Received
- September 29, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Replacement, Ossicular Prosthesis, Total
- Device Class
- Class II
- Regulation Number
- 874.3495
- Review Panel
- EN
- Submission Type