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)

DELFIA NEONATAL IRT KIT

K-Number: K993697 · 2000-06-09

ApplicantWallac OY
Decision Date2000-06-09
Product CodeCGZ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DELFIA NEONATAL IRT KIT is the device name listed in this FDA 510(k) record. The listed applicant is Wallac OY. It received FDA 510(k) clearance on 2000-06-09 under 510(k) number K993697. The device is classified under product code CGZ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DELFIA NEONATAL IRT KIT?

DELFIA NEONATAL IRT KIT is a medical device that received FDA 510(k) clearance on 2000-06-09. The listed applicant is Wallac OY. The 510(k) number is K993697.

When did DELFIA NEONATAL IRT KIT receive FDA 510(k) clearance?

DELFIA NEONATAL IRT KIT received FDA 510(k) clearance on 2000-06-09, under 510(k) number K993697.

Who is the listed applicant for DELFIA NEONATAL IRT KIT?

The FDA 510(k) record lists Wallac OY as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DELFIA NEONATAL IRT KIT?

The FDA product code for DELFIA NEONATAL IRT KIT is CGZ.

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 Wallac OY 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 21 devices →

Related Devices (Code: CGZ)

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.

↑