510(k) K012917

DYNAREX UMBILICAL CORD LAMP, MODELS 6833 AND 6833-B by Dynarex Corp. — Product Code HFW

K012917 is an FDA 510(k) premarket notification submitted by Dynarex Corp. for the device "DYNAREX UMBILICAL CORD LAMP, MODELS 6833 AND 6833-B". The FDA issued a decision of Substantially Equivalent on November 28, 2001. The device falls under product code HFW (Clamp, Umbilical), a Class II device regulated under 21 CFR 884.4530. Dynarex Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 28, 2001
Date Received
August 30, 2001
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Clamp, Umbilical
Device Class
Class II
Regulation Number
884.4530
Review Panel
OB
Submission Type