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FDA 510(k)

MEDI-SIS SYRINGE INFUSION SYSTEM

K-Number: K111381 · 2012-01-13

ApplicantAcacia, Inc.
Decision Date2012-01-13
Product CodeLZH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEDI-SIS SYRINGE INFUSION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Acacia, Inc.. It received FDA 510(k) clearance on 2012-01-13 under 510(k) number K111381. The device is classified under product code LZH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDI-SIS SYRINGE INFUSION SYSTEM?

MEDI-SIS SYRINGE INFUSION SYSTEM is a medical device that received FDA 510(k) clearance on 2012-01-13. The listed applicant is Acacia, Inc.. The 510(k) number is K111381.

When did MEDI-SIS SYRINGE INFUSION SYSTEM receive FDA 510(k) clearance?

MEDI-SIS SYRINGE INFUSION SYSTEM received FDA 510(k) clearance on 2012-01-13, under 510(k) number K111381.

Who is the listed applicant for MEDI-SIS SYRINGE INFUSION SYSTEM?

The FDA 510(k) record lists Acacia, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDI-SIS SYRINGE INFUSION SYSTEM?

The FDA product code for MEDI-SIS SYRINGE INFUSION SYSTEM is LZH.

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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.

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