Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

INNOMED PD-1 KIT

K-Number: K822574 · 1982-10-13

ApplicantInnomed Corp.
Decision Date1982-10-13
Product CodeLJL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INNOMED PD-1 KIT is the device name listed in this FDA 510(k) record. The listed applicant is Innomed Corp.. It received FDA 510(k) clearance on 1982-10-13 under 510(k) number K822574. The device is classified under product code LJL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

↑