510(k) K910676
K910676 is an FDA 510(k) premarket notification submitted by Pemaco, Inc. for the device "INTRAORAL DENTAL WAX". The FDA issued a decision of Substantially Equivalent on August 21, 1991. The device falls under product code EGD (Wax, Dental, Intraoral), a Class I device regulated under 21 CFR 872.6890. Pemaco, Inc. has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 21, 1991
- Date Received
- February 15, 1991
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Wax, Dental, Intraoral
- Device Class
- Class I
- Regulation Number
- 872.6890
- Review Panel
- DE
- Submission Type