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

Alarm, Blood-Pressure

21 CFR 870.1100 / Cardiovascular
FDA source (opens on fda.gov)

DSJ is the FDA product code for Alarm, Blood-Pressure, a class II device type, regulated under 21 CFR 870.1100. As of , FDA records hold 6 510(k) clearances under this code, the most recent dated , and 4 recalls.

Classification record

Product code
DSJ
Device name
Alarm, Blood-Pressure
Regulation
21 CFR 870.1100
Device class
Class II
Review panel
Cardiovascular
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
6
Ingested recalls
4

Clearances, product code DSJ

By decision year
6 clearances under product code DSJ with a decision year between 1991 and 2019, 1991 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code DSJ by decision year
YearClearances
19911
19961
20141
20151
20171
20191

Applicants with the most clearances

Product code DSJ
Applicants holding the most 510(k) clearances under product code DSJ
ApplicantClearances
Philips North America LLC2
3M Health Care, Sarns1
Keller Medical Specialties Products, Inc.1
Philips Medizin Systeme Boeblingen GmbH1
Phillips Medical Systems1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 34 companies shown, in name order