510(k) K922843

DYNAREX SUCTION CATHETERS & KITS by Dynarex Corp. — Product Code BSY

K922843 is an FDA 510(k) premarket notification submitted by Dynarex Corp. for the device "DYNAREX SUCTION CATHETERS & KITS". The FDA issued a decision of Substantially Equivalent on January 11, 1993. The device falls under product code BSY (Catheters, Suction, Tracheobronchial), a Class I device regulated under 21 CFR 868.6810. Dynarex Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 11, 1993
Date Received
June 12, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Catheters, Suction, Tracheobronchial
Device Class
Class I
Regulation Number
868.6810
Review Panel
AN
Submission Type