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FDA 510(k)

ARTERIAL BLOOD SAMPLING KIT

K-Number: K821406 · 1982-06-25

Decision Date1982-06-25
Product CodeCBT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ARTERIAL BLOOD SAMPLING KIT is the device name listed in this FDA 510(k) record. The listed applicant is Dhd Medical Products Div. Diemolding Corp.. It received FDA 510(k) clearance on 1982-06-25 under 510(k) number K821406. 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 ARTERIAL BLOOD SAMPLING KIT?

ARTERIAL BLOOD SAMPLING KIT is a medical device that received FDA 510(k) clearance on 1982-06-25. The listed applicant is Dhd Medical Products Div. Diemolding Corp.. The 510(k) number is K821406.

When did ARTERIAL BLOOD SAMPLING KIT receive FDA 510(k) clearance?

ARTERIAL BLOOD SAMPLING KIT received FDA 510(k) clearance on 1982-06-25, under 510(k) number K821406.

Who is the listed applicant for ARTERIAL BLOOD SAMPLING KIT?

The FDA 510(k) record lists Dhd Medical Products Div. Diemolding Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARTERIAL BLOOD SAMPLING KIT?

The FDA product code for ARTERIAL BLOOD SAMPLING KIT is CBT.

Related Clinical Trials

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.

Other records listing Dhd Medical Products Div. Diemolding 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.

View all 43 devices →

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.

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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