510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K012917Substantially Equivalent

Dynarex Umbilical Cord Lamp, Models 6833 and 6833-B

Dynarex Corp., Maineville OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K012917 is the FDA 510(k) clearance record for DYNAREX UMBILICAL CORD LAMP, MODELS 6833 AND 6833-B, a class II device, cleared for Dynarex Corp. on under FDA product code HFW (Clamp, Umbilical). FDA records list 27 510(k) clearances for Dynarex Corp., from to . As of , FDA records show no recalls naming K012917.

Clearance record

Decision date
Received
(90 days to decision)
Product code
HFW Clamp, Umbilical
Regulation
21 CFR 884.4530
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Dynarex Corp. 7736 Woodside Ct., Maineville OH
510(k) summary
Summary
Third party review
No

Clearances, product code HFW

Trailing 12 months

FDA records hold no clearances under product code HFW in the trailing twelve months.

FDA records show no clearances under product code HFW in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HFW, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260