510(k) K760548
K760548 is an FDA 510(k) premarket notification submitted by Landmark Plastics for the device "CARAFE AND LINER". The FDA issued a decision of Substantially Equivalent on November 12, 1976. Landmark Plastics has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 12, 1976
- Date Received
- August 30, 1976
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No