FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
FORGET - DENTURE BONDING LIQUID
K Number: K791576
·
Decision Oct 26, 1979
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
1
Applicant Total
4
Review Days
70
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Basic Information
- Device Name
- FORGET - DENTURE BONDING LIQUID
- K Number
- K791576
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 872.3410
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Applicant
- Norcliff Thayer, Inc.
- Date Received
- August 17, 1979
- Decision Date
- October 26, 1979
- Product Code
- KOL
- Advisory Committee
- Dental
- Review Advisory Committee
- DE
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| KOL | Adhesive, Denture, Carboxymethylcellulose Sodium (32%) And Ethylene-Oxide Homopolymer | FDA class 1 | Dental |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (KOL), ordered by most recent decision date.
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