510(k) K830572

CLEAN-FLUSH by Burron Medical Products, Inc. — Product Code KYZ

K830572 is an FDA 510(k) premarket notification submitted by Burron Medical Products, Inc. for the device "CLEAN-FLUSH". The FDA issued a decision of Substantially Equivalent on March 17, 1983. The device falls under product code KYZ (Syringe, Irrigating (Non Dental)), a Class I device regulated under 21 CFR 880.6960. Burron Medical Products, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 17, 1983
Date Received
February 23, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Syringe, Irrigating (Non Dental)
Device Class
Class I
Regulation Number
880.6960
Review Panel
HO
Submission Type