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)

TECHNICON DPA-1 ANALYTE ALPHA 1 ACID GLYCOPROTEIN

K-Number: K884217 · 1988-11-04

Decision Date1988-11-04
Product CodeLKL
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

TECHNICON DPA-1 ANALYTE ALPHA 1 ACID GLYCOPROTEIN is the device name listed in this FDA 510(k) record. The listed applicant is Technicon Instruments Corp.. It received FDA 510(k) clearance on 1988-11-04 under 510(k) number K884217. The device is classified under product code LKL. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHNICON DPA-1 ANALYTE ALPHA 1 ACID GLYCOPROTEIN?

TECHNICON DPA-1 ANALYTE ALPHA 1 ACID GLYCOPROTEIN is a medical device that received FDA 510(k) clearance on 1988-11-04. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K884217.

When did TECHNICON DPA-1 ANALYTE ALPHA 1 ACID GLYCOPROTEIN receive FDA 510(k) clearance?

TECHNICON DPA-1 ANALYTE ALPHA 1 ACID GLYCOPROTEIN received FDA 510(k) clearance on 1988-11-04, under 510(k) number K884217.

Who is the listed applicant for TECHNICON DPA-1 ANALYTE ALPHA 1 ACID GLYCOPROTEIN?

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

What is the FDA product code for TECHNICON DPA-1 ANALYTE ALPHA 1 ACID GLYCOPROTEIN?

The FDA product code for TECHNICON DPA-1 ANALYTE ALPHA 1 ACID GLYCOPROTEIN is LKL.

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 Technicon Instruments 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.

View all 157 devices →

Related Devices (Code: LKL)

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.

↑