FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

Pressure Right, Single-Use, Disposable, Acupressure, Pressure-Sensitive Wrist Strip

K Number: K142471 · Decision Dec 1, 2014
Classifications
1
FEI Numbers
9
Registration Numbers
9
Same Product Code
12
Applicant Total
1
Review Days
89

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Pressure Right, Single-Use, Disposable, Acupressure, Pressure-Sensitive Wrist Strip
K Number
K142471
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Pressure Point, Inc.
Date Received
September 3, 2014
Decision Date
December 1, 2014
Product Code
MVV
Advisory Committee
Unknown
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MVV Device, Acupressure

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MVV), ordered by most recent decision date.

View all