510(k) K830343
K830343 is an FDA 510(k) premarket notification submitted by American Hospital Supply Corp. for the device "CONTAINER W/PRIMING SOLUTION". The FDA issued a decision of Substantially Equivalent on March 17, 1983. The device falls under product code KDP (Regulator, Vacuum), a Class II device regulated under 21 CFR 880.6740. American Hospital Supply Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 17, 1983
- Date Received
- February 1, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Regulator, Vacuum
- Device Class
- Class II
- Regulation Number
- 880.6740
- Review Panel
- HO
- Submission Type