SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX
K-Number: K210103 · 2021-07-16
ApplicantLifelong Meditech Private Limited
Decision Date2021-07-16
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX is a medical device manufactured by Lifelong Meditech Private Limited. It received FDA 510(k) clearance on 2021-07-16 under approval number K210103. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX?
SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX is a medical device that received FDA 510(k) clearance on 2021-07-16. It is manufactured by Lifelong Meditech Private Limited. The 510(k) number is K210103.
When was SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX approved by the FDA?
SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX received FDA 510(k) clearance on 2021-07-16, under approval number K210103.
What company makes SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX?
SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX is manufactured by Lifelong Meditech Private Limited.
What is the FDA product code for SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX?
The FDA product code for SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX is FMF.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.