Safeway, Lifelong Premium, Lifelong Matrix

FDA 510(k) K210103 · Lifelong Meditech Private Limited

Substantially Equivalent

510(k) numberK210103

Submission

Device name
Safeway, Lifelong Premium, Lifelong Matrix
Applicant
Lifelong Meditech Private Limited
Gurgaon, IN
Received
January 14, 2021
Decision date
July 16, 2021
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FMF – Syringe, Piston
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5860
Specialty
General Hospital

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More from Instylla, Inc.

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Questions and answers

When was Safeway, Lifelong Premium, Lifelong Matrix cleared by the FDA?

Safeway, Lifelong Premium, Lifelong Matrix (K210103) received a 510(k) decision of Substantially Equivalent on July 16, 2021, 183 days after the submission was received.

What is the product code of K210103?

The FDA product code is FMF – Syringe, Piston, a Class II (moderate risk) device regulated under 21 CFR 880.5860.