FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

First Relief v1

K Number: K202940 · Decision Dec 29, 2020
Classifications
1
FEI Numbers
5
Registration Numbers
5
Same Product Code
5
Applicant Total
14
Review Days
90

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Basic Information

Device Name
First Relief v1
K Number
K202940
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5340
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dyansys, Inc.
Date Received
September 30, 2020
Decision Date
December 29, 2020
Product Code
QHH
Advisory Committee
Gastroenterology, Urology
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
QHH Non-Implanted Nerve Stimulator For Pain Associated With Irritable Bowel Syndrome (Ibs)

Similar 510(k) Clearances

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

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Other Clearances by Dyansys, Inc.

K Number Device Name
K221425 Primary Relief
K221231 Drug Relief v1
K220397 ANSiStim-PP
K213188 Primary Relief
K212859 First Relief
K211971 Drug Relief v1
K173861 Drug Relief
K170391 ANSiStim-PP
K141168 ANSISTIM
K091397 ECSCOPE 200
Search all 14 clearances from Dyansys, Inc. →