MEDI-JECTOR
K-Number: K772129 · 1977-12-08
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Device Summary
Frequently Asked Questions
What is the MEDI-JECTOR?
MEDI-JECTOR is a medical device that received FDA 510(k) clearance on 1977-12-08. The listed applicant is Derata Corp.. The 510(k) number is K772129.
When did MEDI-JECTOR receive FDA 510(k) clearance?
MEDI-JECTOR received FDA 510(k) clearance on 1977-12-08, under 510(k) number K772129.
Who is the listed applicant for MEDI-JECTOR?
The FDA 510(k) record lists Derata Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDI-JECTOR?
The FDA product code for MEDI-JECTOR is KZE.
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 Derata Corp. 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.
Related Devices (Code: KZE)
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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