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FDA 510(k)

DELFIA(TM) FERRITIN KIT

K-Number: K872955 · 1987-08-21

Decision Date1987-08-21
Product CodeJMG
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

DELFIA(TM) FERRITIN KIT is the device name listed in this FDA 510(k) record. The listed applicant is Lkb Instruments, Inc.. It received FDA 510(k) clearance on 1987-08-21 under 510(k) number K872955. The device is classified under product code JMG. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DELFIA(TM) FERRITIN KIT?

DELFIA(TM) FERRITIN KIT is a medical device that received FDA 510(k) clearance on 1987-08-21. The listed applicant is Lkb Instruments, Inc.. The 510(k) number is K872955.

When did DELFIA(TM) FERRITIN KIT receive FDA 510(k) clearance?

DELFIA(TM) FERRITIN KIT received FDA 510(k) clearance on 1987-08-21, under 510(k) number K872955.

Who is the listed applicant for DELFIA(TM) FERRITIN KIT?

The FDA 510(k) record lists Lkb Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DELFIA(TM) FERRITIN KIT?

The FDA product code for DELFIA(TM) FERRITIN KIT is JMG.

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 Lkb Instruments, Inc. 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.

View all 52 devices →

Related Devices (Code: JMG)

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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