FDA 510(k)

IMPROVE BLOOD COLLECTION SET AND IMPROSAFE BLOOD COLLECTION SET

K-Number: K123987 · 2013-08-27

ApplicantInnovative Medical Technologies, Inc.

Decision Date2013-08-27

Product CodeJKA

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

IMPROVE BLOOD COLLECTION SET AND IMPROSAFE BLOOD COLLECTION SET is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Medical Technologies, Inc.. It received FDA 510(k) clearance on 2013-08-27 under 510(k) number K123987. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPROVE BLOOD COLLECTION SET AND IMPROSAFE BLOOD COLLECTION SET?

IMPROVE BLOOD COLLECTION SET AND IMPROSAFE BLOOD COLLECTION SET is a medical device that received FDA 510(k) clearance on 2013-08-27. The listed applicant is Innovative Medical Technologies, Inc.. The 510(k) number is K123987.

When did IMPROVE BLOOD COLLECTION SET AND IMPROSAFE BLOOD COLLECTION SET receive FDA 510(k) clearance?

IMPROVE BLOOD COLLECTION SET AND IMPROSAFE BLOOD COLLECTION SET received FDA 510(k) clearance on 2013-08-27, under 510(k) number K123987.

Who is the listed applicant for IMPROVE BLOOD COLLECTION SET AND IMPROSAFE BLOOD COLLECTION SET?

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

What is the FDA product code for IMPROVE BLOOD COLLECTION SET AND IMPROSAFE BLOOD COLLECTION SET?

The FDA product code for IMPROVE BLOOD COLLECTION SET AND IMPROSAFE BLOOD COLLECTION SET is JKA.

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Other records listing Innovative Medical Technologies, Inc. as applicant

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Related Devices (Code: JKA)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.