510(k) K033293
K033293 is an FDA 510(k) premarket notification submitted by Med-Logics, Inc. for the device "MED-LOGICS, MODEL ML7090". The FDA issued a decision of Substantially Equivalent on January 13, 2004. The device falls under product code HNO (Keratome, Ac-Powered), a Class I device regulated under 21 CFR 886.4370. Med-Logics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 13, 2004
- Date Received
- October 14, 2003
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Keratome, Ac-Powered
- Device Class
- Class I
- Regulation Number
- 886.4370
- Review Panel
- OP
- Submission Type