510(k) K800019
K800019 is an FDA 510(k) premarket notification submitted by Fred Sammons, Inc. for the device "BK-1544 BE OK SCOOP DISK". The FDA issued a decision of Substantially Equivalent on January 21, 1980. The device falls under product code ILC (Utensil, Eating), a Class I device regulated under 21 CFR 890.5050. Fred Sammons, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 21, 1980
- Date Received
- January 2, 1980
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Utensil, Eating
- Device Class
- Class I
- Regulation Number
- 890.5050
- Review Panel
- PM
- Submission Type