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

Prosthesis, Penis, Rigid Rod

21 CFR 876.3630 / Gastroenterology, Urology
FDA source (opens on fda.gov)

FTQ is the FDA product code for Prosthesis, Penis, Rigid Rod, a class II device type, regulated under 21 CFR 876.3630. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
FTQ
Device name
Prosthesis, Penis, Rigid Rod
Regulation
21 CFR 876.3630
Device class
Class II
Review panel
Gastroenterology, Urology
Submission type
510(k)
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
2
Ingested recalls
0

Clearances, product code FTQ

By decision year
2 clearances under product code FTQ with a decision year between 1983 and 1999, 1983 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FTQ by decision year
YearClearances
19831
19991

Applicants with the most clearances

Product code FTQ
Applicants holding the most 510(k) clearances under product code FTQ
ApplicantClearances
Dacomed Corp.1
Specialty Surgical Products, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code FTQ.