accufit
K-Number: K223802 · 2023-10-06
ApplicantMettler Electronics Corporation
Decision Date2023-10-06
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
accufit is a medical device manufactured by Mettler Electronics Corporation. It received FDA 510(k) clearance on 2023-10-06 under approval number K223802. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the accufit?
accufit is a medical device that received FDA 510(k) clearance on 2023-10-06. It is manufactured by Mettler Electronics Corporation. The 510(k) number is K223802.
When was accufit approved by the FDA?
accufit received FDA 510(k) clearance on 2023-10-06, under approval number K223802.
What company makes accufit?
accufit is manufactured by Mettler Electronics Corporation.
What is the FDA product code for accufit?
The FDA product code for accufit is IPF.
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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.