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

Seal, Cervical, Mechanical, Unpowered

21 CFR 884.1690 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

QHZ is the FDA product code for Seal, Cervical, Mechanical, Unpowered, a class I device type, regulated under 21 CFR 884.1690. FDA's definition for this code reads: "Reduce fluid leakage from the cervix during hysteroscopic procedures". As of , FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code
QHZ
Device name
Seal, Cervical, Mechanical, Unpowered
FDA definition
Reduce fluid leakage from the cervix during hysteroscopic procedures.
Regulation
21 CFR 884.1690
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
0

Companies listing this code with FDA

Companies whose registered establishments list this code