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

Fluid Jet Removal System

21 CFR 876.4350 / General, Plastic Surgery
FDA source (opens on fda.gov)

PZP is the FDA product code for Fluid Jet Removal System, a class II device type, regulated under 21 CFR 876.4350. FDA's definition for this code reads: "The system is used for removal of prostate tissue with a fluid jet". As of , FDA records hold 9 510(k) clearances under this code, the most recent dated , and 2 recalls.

Classification record

Product code
PZP
Device name
Fluid Jet Removal System
FDA definition
The system is used for removal of prostate tissue with a fluid jet.
Regulation
21 CFR 876.4350
Device class
Class II
Review panel
General, Plastic Surgery
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
9
Ingested recalls
2

Clearances, product code PZP

By decision year
9 clearances under product code PZP with a decision year between 2017 and 2026, 2021 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code PZP by decision year
YearClearances
20171
20212
20231
20242
20251
20262

Applicants with the most clearances

Product code PZP
Applicants holding the most 510(k) clearances under product code PZP
ApplicantClearances
PROCEPT BioRobotics Corporation9

Companies listing this code with FDA

Companies whose registered establishments list this code