inforMED
OHDClass II

Gynecological Laparoscopic Kit

Obstetrics/Gynecology · 21 CFR 884.1720

This product code has been established in accordance with the may 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at www.Fda.Gov/cdrh/ode/convkit.Html. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.

MDR events330All time
Recalls52All time
Registered firms29Currently listed
510(k) clearances0All time

Product problems

Reported product problem codes, most common first

Adverse Event Without Identified Device or Use Problem249
Contamination /Decontamination Problem7
Torn Material7
Break6
Component Missing6
Material Integrity Problem5
Appropriate Device Problem Term/Code Not Available4
Fluid/Blood Leak3

Trend for “Adverse Event Without Identified Device or Use Problem

011Mar 24Apr 24May 24Jun 24Jul 24

Recalls

52 recall events for this product code

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510(k) clearances

0 clearances for this product code

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No 510(k) clearances on file for this product code.