510(k) K792227
K792227 is an FDA 510(k) premarket notification submitted by National Patent Development Corp. for the device "MULTI-AD FLUID DISPENSING SYSTEM". The FDA issued a decision of Substantially Equivalent on December 20, 1979. The device falls under product code KYX (Dispenser, Liquid Medication), a Class I device regulated under 21 CFR 880.6430. National Patent Development Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 20, 1979
- Date Received
- November 5, 1979
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Dispenser, Liquid Medication
- Device Class
- Class I
- Regulation Number
- 880.6430
- Review Panel
- HO
- Submission Type