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

Table, Cystometric, Electric

21 CFR 876.4890 / Gastroenterology, Urology
FDA source (opens on fda.gov)

MMZ is the FDA product code for Table, Cystometric, Electric, a class II device type, regulated under 21 CFR 876.4890. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and 5 recalls.

Classification record

Product code
MMZ
Device name
Table, Cystometric, Electric
Regulation
21 CFR 876.4890
Device class
Class II
Review panel
Gastroenterology, Urology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
4
Ingested recalls
5

Clearances, product code MMZ

By decision year
4 clearances under product code MMZ with a decision year between 1994 and 2003, 1994 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code MMZ by decision year
YearClearances
19942
19951
20031

Applicants with the most clearances

Product code MMZ
Applicants holding the most 510(k) clearances under product code MMZ
ApplicantClearances
Beta Medical Products Co.1
Mdt Corp., Inc.1
Siemens Medical Solutions USA, Inc.1
Synectics Medical, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 14 companies shown, in name order