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FDA 510(k)

BLOOD GAS KIT (NON-STERILE) REORDER NO. 0560

K-Number: K930986 · 1993-07-14

ApplicantCustomed, Inc.
Decision Date1993-07-14
Product CodeCBT
Advisory CommitteeAN
DecisionUnknown

Device Summary

BLOOD GAS KIT (NON-STERILE) REORDER NO. 0560 is the device name listed in this FDA 510(k) record. The listed applicant is Customed, Inc.. It received FDA 510(k) clearance on 1993-07-14 under 510(k) number K930986. The device is classified under product code CBT. It was reviewed by the AN advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the BLOOD GAS KIT (NON-STERILE) REORDER NO. 0560?

BLOOD GAS KIT (NON-STERILE) REORDER NO. 0560 is a medical device that received FDA 510(k) clearance on 1993-07-14. The listed applicant is Customed, Inc.. The 510(k) number is K930986.

When did BLOOD GAS KIT (NON-STERILE) REORDER NO. 0560 receive FDA 510(k) clearance?

BLOOD GAS KIT (NON-STERILE) REORDER NO. 0560 received FDA 510(k) clearance on 1993-07-14, under 510(k) number K930986.

Who is the listed applicant for BLOOD GAS KIT (NON-STERILE) REORDER NO. 0560?

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

What is the FDA product code for BLOOD GAS KIT (NON-STERILE) REORDER NO. 0560?

The FDA product code for BLOOD GAS KIT (NON-STERILE) REORDER NO. 0560 is CBT.

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Other records listing Customed, 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.

K974647FANFOLD DRAPE 41 X 57 PRODUCT NO. 900-633, RECORDER NO. 0633K971920GOWN POLY REINFORCED LARGE(PRODUCT NO.900-522)/(REORDER NO. 0522)K964011SUCTION CATHETER TRAY PRODUCT NO. 900277K962652URINARY DRAINAGE BAG, (REORDER NO. 0749 - PRODUCT NO. 900-749)K962596CUSTOMED BLOOD EXTRACTION KITK961442UNIVERSAL DRAINAGE TRAY

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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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