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

System, Pressure Measurement, Intermittent

21 CFR 890.1600 / Physical Medicine
FDA source (opens on fda.gov)

JFC is the FDA product code for System, Pressure Measurement, Intermittent, a class I device type, regulated under 21 CFR 890.1600. As of , FDA records hold 11 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
JFC
Device name
System, Pressure Measurement, Intermittent
Regulation
21 CFR 890.1600
Device class
Class I
Review panel
Physical Medicine
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
11
Ingested recalls
1

Clearances, product code JFC

By decision year
11 clearances under product code JFC with a decision year between 1983 and 1993, 1993 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code JFC by decision year
YearClearances
19832
19861
19882
19912
19921
19933

Applicants with the most clearances

Product code JFC
Applicants holding the most 510(k) clearances under product code JFC
ApplicantClearances
Pin Dot Products, Inc.2
Biokinetics, Inc.1
Electromedics, Inc.1
Force Sensing Systems1
Gabel Medical Instruments, Ltd.1
Human Performance Technologies, Inc.1
Nathaniel Gould Diagnostics, Inc.1
Talley Group Ltd.1
Tee-Kay Applied Technology1
Wrm Computers1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 39 companies shown, in name order