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

Microscope And Microscope Accessories, Reproduction, Assisted

21 CFR 884.6190 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

MTX is the FDA product code for Microscope And Microscope Accessories, Reproduction, Assisted, a class I device type, regulated under 21 CFR 884.6190. As of , FDA records hold no 510(k) clearances under this code and one recall.

Classification record

Product code
MTX
Device name
Microscope And Microscope Accessories, Reproduction, Assisted
Regulation
21 CFR 884.6190
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 17 companies shown, in name order