Invu By Nuvo

Home Uterine Activity Monitor

Nuvo- Group Ltd.

The following data is part of a premarket notification filed by Nuvo- Group Ltd. with the FDA for Invu By Nuvo.

Pre-market Notification Details

Device IDK221046
510k NumberK221046
Device Name:Invu By Nuvo
ClassificationHome Uterine Activity Monitor
Applicant Nuvo- Group Ltd. Yigal Alon 94. St, Alon Tower 1 Tel Aviv,  IL 6789155
ContactChen Rubinstein
CorrespondentJanice Hogan
Hogan Lovells US LLP 1735 Market St., 23rd Floor Philladelphia,  PA  19103
Product CodeLQK  
CFR Regulation Number884.2730 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2022-04-08
Decision Date2022-05-06

Trademark Results [Invu By Nuvo]

Mark Image

Registration | Serial
Company
Trademark
Application Date
INVU BY NUVO
INVU BY NUVO
79292705 not registered Live/Pending
NUVO GROUP LTD
2020-05-12

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