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

Tubing And Tubing/Filter Fits

21 CFR 884.1700 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

NVT is the FDA product code for Tubing And Tubing/Filter Fits, a class I device type, regulated under 21 CFR 884.1700. FDA's definition for this code reads: "Tubing and tubing/filter fits are used when there is a need to distend the uterus by filling the uterine cavity with a liquid or gas to facilitate viewing with a hysteroscope". As of , FDA records hold no 510(k) clearances under this code and one recall.

Classification record

Product code
NVT
Device name
Tubing And Tubing/Filter Fits
FDA definition
Tubing and tubing/filter fits are used when there is a need to distend the uterus by filling the uterine cavity with a liquid or gas to facilitate viewing with a hysteroscope.
Regulation
21 CFR 884.1700
Device class
Class I
Review panel
Obstetrics/Gynecology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 15 companies shown, in name order