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FDA 510(k)

HYPODERMIC JET INJECTION APPARATUS

K-Number: K962017 · 1996-07-26

Decision Date1996-07-26
Product CodeEGM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HYPODERMIC JET INJECTION APPARATUS is the device name listed in this FDA 510(k) record. The listed applicant is American Jet Injector Corp.. It received FDA 510(k) clearance on 1996-07-26 under 510(k) number K962017. The device is classified under product code EGM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYPODERMIC JET INJECTION APPARATUS?

HYPODERMIC JET INJECTION APPARATUS is a medical device that received FDA 510(k) clearance on 1996-07-26. The listed applicant is American Jet Injector Corp.. The 510(k) number is K962017.

When did HYPODERMIC JET INJECTION APPARATUS receive FDA 510(k) clearance?

HYPODERMIC JET INJECTION APPARATUS received FDA 510(k) clearance on 1996-07-26, under 510(k) number K962017.

Who is the listed applicant for HYPODERMIC JET INJECTION APPARATUS?

The FDA 510(k) record lists American Jet Injector Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HYPODERMIC JET INJECTION APPARATUS?

The FDA product code for HYPODERMIC JET INJECTION APPARATUS is EGM.

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.

Related Devices (Code: EGM)

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

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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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