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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Lifelong Meditech Private Limited. It received FDA 510(k) clearance on 2021-07-16 under 510(k) 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. The listed applicant is Lifelong Meditech Private Limited. The 510(k) number is K210103.

When did SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX receive FDA 510(k) clearance?

SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX received FDA 510(k) clearance on 2021-07-16, under 510(k) number K210103.

Who is the listed applicant for SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX?

The FDA 510(k) record lists Lifelong Meditech Private Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX?

The FDA product code for SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX is FMF.

Other records listing Lifelong Meditech Private Limited as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K222925Hypodermic Syringes & Needle

Related Devices (Code: FMF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253747Disposable Pen Injector (KXYC-03C02, KXYC-03A03)Jiangsu Enjosim Medical Technology Co., Ltd.K260208Ultra-Fine™ SAFETY Insulin Syringeembecta Medical II, LLCK253110Sol-Glide Safety Needle; Sol-Glide Safety Needle with SyringeSol-Millennium Medical, Inc.K260514Profoject™ Safety Needle; Profoject™ Syringe with Safety Needle; Profoject™ Low Dead Space Syringe with Safety NeedleCMT Health PTE., Ltd.K253112Sofjec (Single use Needle); Sofjec (Single use Syringe with or without Needle); Sofjec (Membrane Filter Syringe)Hlb Lifescience Co., Ltd.K252279Sterile Hypodermic Syringe for Single Use (20ml, 30ml, 50ml, 60ml)Chirana T.Injecta,A.S.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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