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FDA 510(k)

MODEL 1050 - UMBILICAL CORD BLOOD SAMPLING KIT

K-Number: K897133 · 1990-03-30

ApplicantTransidyne General Corp.
Decision Date1990-03-30
Product CodeCBT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODEL 1050 - UMBILICAL CORD BLOOD SAMPLING KIT is the device name listed in this FDA 510(k) record. The listed applicant is Transidyne General Corp.. It received FDA 510(k) clearance on 1990-03-30 under 510(k) number K897133. 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 MODEL 1050 - UMBILICAL CORD BLOOD SAMPLING KIT?

MODEL 1050 - UMBILICAL CORD BLOOD SAMPLING KIT is a medical device that received FDA 510(k) clearance on 1990-03-30. The listed applicant is Transidyne General Corp.. The 510(k) number is K897133.

When did MODEL 1050 - UMBILICAL CORD BLOOD SAMPLING KIT receive FDA 510(k) clearance?

MODEL 1050 - UMBILICAL CORD BLOOD SAMPLING KIT received FDA 510(k) clearance on 1990-03-30, under 510(k) number K897133.

Who is the listed applicant for MODEL 1050 - UMBILICAL CORD BLOOD SAMPLING KIT?

The FDA 510(k) record lists Transidyne General Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL 1050 - UMBILICAL CORD BLOOD SAMPLING KIT?

The FDA product code for MODEL 1050 - UMBILICAL CORD BLOOD SAMPLING KIT is CBT.

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Other records listing Transidyne General Corp. 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.

K961217BODILY FLUID DISPOSAL KITK955658LACERATION TRAYK950743ORAL PROCEDURE PACKK950773PROPHYLAXIS PACKK950449SURGICAL BURK950403SURGICAL SAW BLADES

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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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