510(k) K925259
K925259 is an FDA 510(k) premarket notification submitted by Combe, Inc. for the device "CFR MONOGRAPH". The FDA issued a decision of Substantially Equivalent on January 11, 1993. The device falls under product code EFT (Cleanser, Denture, Over The Counter), a Class I device regulated under 21 CFR 872.3520. Combe, Inc. has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 11, 1993
- Date Received
- October 19, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Cleanser, Denture, Over The Counter
- Device Class
- Class I
- Regulation Number
- 872.3520
- Review Panel
- DE
- Submission Type