FDA 510(k)

NON-KOR WINGED INFUSION SETS

K-Number: K861406 · 1986-05-06

Decision Date1986-05-06

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

NON-KOR WINGED INFUSION SETS is the device name listed in this FDA 510(k) record. The listed applicant is Creative Care Systems, Inc.. It received FDA 510(k) clearance on 1986-05-06 under 510(k) number K861406. 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 NON-KOR WINGED INFUSION SETS?

NON-KOR WINGED INFUSION SETS is a medical device that received FDA 510(k) clearance on 1986-05-06. The listed applicant is Creative Care Systems, Inc.. The 510(k) number is K861406.

When did NON-KOR WINGED INFUSION SETS receive FDA 510(k) clearance?

NON-KOR WINGED INFUSION SETS received FDA 510(k) clearance on 1986-05-06, under 510(k) number K861406.

Who is the listed applicant for NON-KOR WINGED INFUSION SETS?

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

What is the FDA product code for NON-KOR WINGED INFUSION SETS?

The FDA product code for NON-KOR WINGED INFUSION SETS is FMI.

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Other records listing Creative Care Systems, Inc. as applicant

K852831NON-KOR ACCESS KITS K850888PERCUTANEOUS CV CATHETER INSERTION KIT W OR W/O CV K850887DRESSING CHANGE KIT K841742NON-CORING NEEDLE K840919DAYPAK SYS VII CATHETER CARE KIT K840681DAYPAK SYSTEM III CATHETER CARE KIT

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Related Devices (Code: FMI)

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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.