510(k) K972131
K972131 is an FDA 510(k) premarket notification submitted by Beyond 21st Century, Inc. for the device "BREATH ACE BREATHFRESHENER". The FDA issued a decision of Substantially Equivalent on July 18, 1997. The device falls under product code LCN (Scraper, Tongue), a Class I device regulated under 21 CFR 872.6855.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 18, 1997
- Date Received
- June 6, 1997
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Scraper, Tongue
- Device Class
- Class I
- Regulation Number
- 872.6855
- Review Panel
- DE
- Submission Type