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FDA 510(k)

CORD-ASSURE UMBILICAL BLOOD GAS KIT

K-Number: K872244 · 1987-07-21

ApplicantLake Medical Products, Inc.
Decision Date1987-07-21
Product CodeCBT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CORD-ASSURE UMBILICAL BLOOD GAS KIT is the device name listed in this FDA 510(k) record. The listed applicant is Lake Medical Products, Inc.. It received FDA 510(k) clearance on 1987-07-21 under 510(k) number K872244. The device is classified under product code CBT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORD-ASSURE UMBILICAL BLOOD GAS KIT?

CORD-ASSURE UMBILICAL BLOOD GAS KIT is a medical device that received FDA 510(k) clearance on 1987-07-21. The listed applicant is Lake Medical Products, Inc.. The 510(k) number is K872244.

When did CORD-ASSURE UMBILICAL BLOOD GAS KIT receive FDA 510(k) clearance?

CORD-ASSURE UMBILICAL BLOOD GAS KIT received FDA 510(k) clearance on 1987-07-21, under 510(k) number K872244.

Who is the listed applicant for CORD-ASSURE UMBILICAL BLOOD GAS KIT?

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

What is the FDA product code for CORD-ASSURE UMBILICAL BLOOD GAS KIT?

The FDA product code for CORD-ASSURE UMBILICAL BLOOD GAS KIT is CBT.

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Other records listing Lake Medical Products, 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.

K943162LAKE STAGEZERO(TM) AIR FLOTATION BEDK922730LAKE OSTOMY CARE SETK905053STAGE ZERO AIR FLOTATION BEDK901835LAKE N/G FEEDING TUBE (WITH Y PORT CONNECTOR)K902508LAKE MALE EXTERNAL CATHETERIZATION KITK902121LAKE GASTROSTOMY TUBE

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Related Devices (Code: CBT)

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.

K071269HEMODRAW ARTERIAL BLOOD SAMPLING SYSTEMSmiths Medical Asd, Inc.K070340SECURE ARTERIAL BLOOD SAMPLING SYSTEMSmiths Medical Asd, Inc.K955663ABC IN-LINE BLOOD SAMPLING KITUtah Medical Products, Inc.K954015ABG POINT LOK NEEDLE PROTECTION DEVICEDevon Industries, Inc.K954035ACTI-FLEX ARTERIAL EXTENSION SETR-Group Intl.K950098NEEDLE SAFETY COVERHammer-Plane, Inc.

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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