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

Lubricant, Vaginal, Patient

21 CFR 880.6375 / General Hospital
FDA source (opens on fda.gov)

MMS is the FDA product code for Lubricant, Vaginal, Patient, a class I device type, regulated under 21 CFR 880.6375. As of , FDA records hold no 510(k) clearances under this code and 2 recalls.

Classification record

Product code
MMS
Device name
Lubricant, Vaginal, Patient
Regulation
21 CFR 880.6375
Device class
Class I
Review panel
General Hospital
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
0
Ingested recalls
2

Companies listing this code with FDA

Companies whose registered establishments list this code