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FDA 510(k)

RELI Safety Blood Collection Tube Holder, RELI Blood Collection Tube Holder

K-Number: K173279 · 2018-05-14

ApplicantMyco Medical Supplies, Inc.
Decision Date2018-05-14
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RELI Safety Blood Collection Tube Holder, RELI Blood Collection Tube Holder is a medical device manufactured by Myco Medical Supplies, Inc.. It received FDA 510(k) clearance on 2018-05-14 under approval number K173279. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RELI Safety Blood Collection Tube Holder, RELI Blood Collection Tube Holder?

RELI Safety Blood Collection Tube Holder, RELI Blood Collection Tube Holder is a medical device that received FDA 510(k) clearance on 2018-05-14. It is manufactured by Myco Medical Supplies, Inc.. The 510(k) number is K173279.

When was RELI Safety Blood Collection Tube Holder, RELI Blood Collection Tube Holder approved by the FDA?

RELI Safety Blood Collection Tube Holder, RELI Blood Collection Tube Holder received FDA 510(k) clearance on 2018-05-14, under approval number K173279.

What company makes RELI Safety Blood Collection Tube Holder, RELI Blood Collection Tube Holder?

RELI Safety Blood Collection Tube Holder, RELI Blood Collection Tube Holder is manufactured by Myco Medical Supplies, Inc..

What is the FDA product code for RELI Safety Blood Collection Tube Holder, RELI Blood Collection Tube Holder?

The FDA product code for RELI Safety Blood Collection Tube Holder, RELI Blood Collection Tube Holder is FMI.

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Related PubMed Literature

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Other Devices by Myco Medical Supplies, Inc.

K203668RELI NRFit Epidural Needles, Phoenix NRFit Epidural Needles, RELI NRFit Spinal Needles, Phoenix NRFit Spinal Needles

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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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