INNOMED PD-1 KIT
K-Number: K822574 · 1982-10-13
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Device Summary
Frequently Asked Questions
What is the INNOMED PD-1 KIT?
INNOMED PD-1 KIT is a medical device that received FDA 510(k) clearance on 1982-10-13. The listed applicant is Innomed Corp.. The 510(k) number is K822574.
When did INNOMED PD-1 KIT receive FDA 510(k) clearance?
INNOMED PD-1 KIT received FDA 510(k) clearance on 1982-10-13, under 510(k) number K822574.
Who is the listed applicant for INNOMED PD-1 KIT?
The FDA 510(k) record lists Innomed Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INNOMED PD-1 KIT?
The FDA product code for INNOMED PD-1 KIT is LJL.
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 Innomed 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: LJL)
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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