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FDA 510(k)

DAYPAK SYS VII CATHETER CARE KIT

K-Number: K840919 · 1984-04-17

ApplicantCreative Care Systems, Inc.
Decision Date1984-04-17
Product CodeKLK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DAYPAK SYS VII CATHETER CARE KIT 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 1984-04-17 under 510(k) number K840919. The device is classified under product code KLK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAYPAK SYS VII CATHETER CARE KIT?

DAYPAK SYS VII CATHETER CARE KIT is a medical device that received FDA 510(k) clearance on 1984-04-17. The listed applicant is Creative Care Systems, Inc.. The 510(k) number is K840919.

When did DAYPAK SYS VII CATHETER CARE KIT receive FDA 510(k) clearance?

DAYPAK SYS VII CATHETER CARE KIT received FDA 510(k) clearance on 1984-04-17, under 510(k) number K840919.

Who is the listed applicant for DAYPAK SYS VII CATHETER CARE KIT?

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 DAYPAK SYS VII CATHETER CARE KIT?

The FDA product code for DAYPAK SYS VII CATHETER CARE KIT is KLK.

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Other records listing Creative Care Systems, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K861406NON-KOR WINGED INFUSION SETSK852831NON-KOR ACCESS KITSK850888PERCUTANEOUS CV CATHETER INSERTION KIT W OR W/O CVK850887DRESSING CHANGE KITK841742NON-CORING NEEDLEK840681DAYPAK SYSTEM III CATHETER CARE KIT

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Related Devices (Code: KLK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K003943MICROGAS 7650 TRANSCUTANEOUS MONITORLinde Medical Sensors AGK991644MICROGAS 7650 TRANSCUTANEOUS MONITORLinde Medical Sensors AGK980287SIEMENS SC9000/SC9015 TCP02/C02 MODULESiemens Medical Solutions USA, Inc.K924709SATCARE OXYGEN CONTROLLER/MONITOR W/ PULSE OXIMETEAir-Shields, Inc.K924679OXYCARE(TM) OXYGEN CONTROLLER/MONITORAir-Shields Vickers, Inc.K925910HEWLETT-PACKARD MODEL M1018A TCPO2/TOPCO2 MODULEHewlett-Packard Co.

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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