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

Reprocessed Blood Pressure Cuff

21 CFR 870.1120 / Cardiovascular
FDA source (opens on fda.gov)

NPP is the FDA product code for Reprocessed Blood Pressure Cuff, a class II device type, regulated under 21 CFR 870.1120. FDA's definition for this code reads: "The intended use for the reprocessed/reused blood pressure cuff is use in manual measurement and automatic non-invasive blood pressure monitoring by properly trained personnel. Complete inflation systems are designed for use with manometers during manual bp measurement". As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
NPP
Device name
Reprocessed Blood Pressure Cuff
FDA definition
The intended use for the reprocessed/reused blood pressure cuff is use in manual measurement and automatic non-invasive blood pressure monitoring by properly trained personnel. Complete inflation systems are designed for use with manometers during manual bp measurement.
Regulation
21 CFR 870.1120
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
1
Ingested recalls
0

Clearances, product code NPP

By decision year
1 clearance under product code NPP with a decision year between 2003 and 2003, 2003 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code NPP by decision year
YearClearances
20031

Applicants with the most clearances

Product code NPP
Applicants holding the most 510(k) clearances under product code NPP
ApplicantClearances
Hygia Health Services, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code