510(k) K830546

DOSIMETRIC RELEASE by American Hospital Supply Corp. — Product Code KQT

K830546 is an FDA 510(k) premarket notification submitted by American Hospital Supply Corp. for the device "DOSIMETRIC RELEASE". The FDA issued a decision of Substantially Equivalent on May 25, 1983. The device falls under product code KQT (Evacuator, Gastro-Urology), a Class II device regulated under 21 CFR 876.4370. American Hospital Supply Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 25, 1983
Date Received
February 22, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Evacuator, Gastro-Urology
Device Class
Class II
Regulation Number
876.4370
Review Panel
GU
Submission Type