510(k) K791576
K791576 is an FDA 510(k) premarket notification submitted by Norcliff Thayer, Inc. for the device "FORGET - DENTURE BONDING LIQUID". The FDA issued a decision of Substantially Equivalent on October 26, 1979. The device falls under product code KOL (Adhesive, Denture, Carboxymethylcellulose Sodium (32%) And Ethylene-Oxide Homopolymer), a Class I device regulated under 21 CFR 872.3410. Norcliff Thayer, Inc. has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 26, 1979
- Date Received
- August 17, 1979
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Adhesive, Denture, Carboxymethylcellulose Sodium (32%) And Ethylene-Oxide Homopolymer
- Device Class
- Class I
- Regulation Number
- 872.3410
- Review Panel
- DE
- Submission Type