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FDA 510(k)

ARTERIAL LINE KIT

K-Number: K822760 · 1982-09-28

Decision Date1982-09-28
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ARTERIAL LINE KIT is the device name listed in this FDA 510(k) record. The listed applicant is Martell Medical Products, Inc.. It received FDA 510(k) clearance on 1982-09-28 under 510(k) number K822760. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTERIAL LINE KIT?

ARTERIAL LINE KIT is a medical device that received FDA 510(k) clearance on 1982-09-28. The listed applicant is Martell Medical Products, Inc.. The 510(k) number is K822760.

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

ARTERIAL LINE KIT received FDA 510(k) clearance on 1982-09-28, under 510(k) number K822760.

Who is the listed applicant for ARTERIAL LINE KIT?

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

What is the FDA product code for ARTERIAL LINE KIT?

The FDA product code for ARTERIAL LINE KIT is FMF.

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 Martell 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.

View all 7 devices →

Related Devices (Code: FMF)

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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