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FDA 510(k)

E-Z-JECTOR

K-Number: K780883 · 1978-08-10

ApplicantHarco Products
Decision Date1978-08-10
Product CodeKZA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

E-Z-JECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Harco Products. It received FDA 510(k) clearance on 1978-08-10 under 510(k) number K780883. The device is classified under product code KZA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the E-Z-JECTOR?

E-Z-JECTOR is a medical device that received FDA 510(k) clearance on 1978-08-10. The listed applicant is Harco Products. The 510(k) number is K780883.

When did E-Z-JECTOR receive FDA 510(k) clearance?

E-Z-JECTOR received FDA 510(k) clearance on 1978-08-10, under 510(k) number K780883.

Who is the listed applicant for E-Z-JECTOR?

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

What is the FDA product code for E-Z-JECTOR?

The FDA product code for E-Z-JECTOR is KZA.

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.

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Other records listing Harco Products 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.

K780884HYPO-GRIP

Related Devices (Code: KZA)

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.

K152088IV-eyeNovarix LimitedK101838VTS1000Vuetek Scientific, LLCK042679IR VIEWERInfrared Imaging Systems, Inc.K982612ESP7 VENOUS IMAGEIronmaster, Inc.K780884HYPO-GRIPHarco Products

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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