Insulin Syringe
K-Number: K233794 · 2024-03-06
ApplicantSpm Medicare Pvt. , Ltd.
Decision Date2024-03-06
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Insulin Syringe is a medical device manufactured by Spm Medicare Pvt. , Ltd.. It received FDA 510(k) clearance on 2024-03-06 under approval number K233794. 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 Insulin Syringe?
Insulin Syringe is a medical device that received FDA 510(k) clearance on 2024-03-06. It is manufactured by Spm Medicare Pvt. , Ltd.. The 510(k) number is K233794.
When was Insulin Syringe approved by the FDA?
Insulin Syringe received FDA 510(k) clearance on 2024-03-06, under approval number K233794.
What company makes Insulin Syringe?
Insulin Syringe is manufactured by Spm Medicare Pvt. , Ltd..
What is the FDA product code for Insulin Syringe?
The FDA product code for Insulin Syringe is FMF.
Related Clinical Trials
Other Devices by Spm Medicare Pvt. , Ltd.
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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.