HYPODERMIC JET INJECTION APPARATUS
K-Number: K962017 · 1996-07-26
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Device Summary
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
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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