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

Bathophenanthroline, Iron Binding Capacity

21 CFR 862.1415 / Clinical Chemistry
FDA source (opens on fda.gov)

JQF is the FDA product code for Bathophenanthroline, Iron Binding Capacity, a class I device type, regulated under 21 CFR 862.1415. As of , FDA records hold 8 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
JQF
Device name
Bathophenanthroline, Iron Binding Capacity
Regulation
21 CFR 862.1415
Device class
Class I
Review panel
Clinical Chemistry
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
8
Ingested recalls
0

Clearances, product code JQF

By decision year
8 clearances under product code JQF with a decision year between 1979 and 2005, 1981 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code JQF by decision year
YearClearances
19791
19812
19831
19861
19881
19991
20051

Applicants with the most clearances

Product code JQF
Applicants holding the most 510(k) clearances under product code JQF
ApplicantClearances
FUJIFILM Healthcare Americas Corporation2
Bio-Analytics Laboratories, Inc.1
J. D. Assoc.1
Sclavo, Inc.1
Sentinel CH SpA1
Thyroid Diagnostics, Inc.1
Volu Sol Medical Industries1

Companies listing this code with FDA

Companies whose registered establishments list this code