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

Pump, Infusion, Analytical Sampling

21 CFR 880.5725 / General Hospital
FDA source (opens on fda.gov)

LZF is the FDA product code for Pump, Infusion, Analytical Sampling, a class II device type, regulated under 21 CFR 880.5725. As of , FDA records hold 7 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
LZF
Device name
Pump, Infusion, Analytical Sampling
Regulation
21 CFR 880.5725
Device class
Class II
Review panel
General Hospital
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
7
Ingested recalls
1

Clearances, product code LZF

By decision year
7 clearances under product code LZF with a decision year between 1988 and 2020, 1988 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LZF by decision year
YearClearances
19881
19931
19941
19961
20021
20171
20201

Applicants with the most clearances

Product code LZF
Applicants holding the most 510(k) clearances under product code LZF
ApplicantClearances
Via Medical Corp.3
Optiscan Biomedical Corp.2
Metracor Technologies, Inc.1
Pemlab Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code