Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ARTERIAL BLOOD SAMPLING KIT

K-Number: K802185 · 1980-10-10

Decision Date1980-10-10
Product CodeFMP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ARTERIAL BLOOD SAMPLING KIT is the device name listed in this FDA 510(k) record. The listed applicant is Current Technologies, Inc.. It received FDA 510(k) clearance on 1980-10-10 under 510(k) number K802185. The device is classified under product code FMP. It was reviewed by the HO 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 1980-10-10. The listed applicant is Current Technologies, Inc.. The 510(k) number is K802185.

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

ARTERIAL BLOOD SAMPLING KIT received FDA 510(k) clearance on 1980-10-10, under 510(k) number K802185.

Who is the listed applicant for ARTERIAL BLOOD SAMPLING KIT?

The FDA 510(k) record lists Current Technologies, Inc. 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 FMP.

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 Current Technologies, 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.

Related Devices (Code: FMP)

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.

↑