510(k) K830343

CONTAINER W/PRIMING SOLUTION by American Hospital Supply Corp. — Product Code KDP

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