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FDA 510(k)

CATHETER METAL HUB/NONRADIOPAQUE

K-Number: K790968 · 1979-06-11

Decision Date1979-06-11
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CATHETER METAL HUB/NONRADIOPAQUE is the device name listed in this FDA 510(k) record. The listed applicant is Jelco Laboratories. It received FDA 510(k) clearance on 1979-06-11 under 510(k) number K790968. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATHETER METAL HUB/NONRADIOPAQUE?

CATHETER METAL HUB/NONRADIOPAQUE is a medical device that received FDA 510(k) clearance on 1979-06-11. The listed applicant is Jelco Laboratories. The 510(k) number is K790968.

When did CATHETER METAL HUB/NONRADIOPAQUE receive FDA 510(k) clearance?

CATHETER METAL HUB/NONRADIOPAQUE received FDA 510(k) clearance on 1979-06-11, under 510(k) number K790968.

Who is the listed applicant for CATHETER METAL HUB/NONRADIOPAQUE?

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

What is the FDA product code for CATHETER METAL HUB/NONRADIOPAQUE?

The FDA product code for CATHETER METAL HUB/NONRADIOPAQUE is FOZ.

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 Jelco Laboratories 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 26 devices →

Related Devices (Code: FOZ)

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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