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)

PYLORITEK VP TEST KIT 5140VP

K-Number: K014038 · 2002-02-08

Decision Date2002-02-08
Product CodeLYR
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

PYLORITEK VP TEST KIT 5140VP is the device name listed in this FDA 510(k) record. The listed applicant is Serim Research Corp.. It received FDA 510(k) clearance on 2002-02-08 under 510(k) number K014038. The device is classified under product code LYR. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PYLORITEK VP TEST KIT 5140VP?

PYLORITEK VP TEST KIT 5140VP is a medical device that received FDA 510(k) clearance on 2002-02-08. The listed applicant is Serim Research Corp.. The 510(k) number is K014038.

When did PYLORITEK VP TEST KIT 5140VP receive FDA 510(k) clearance?

PYLORITEK VP TEST KIT 5140VP received FDA 510(k) clearance on 2002-02-08, under 510(k) number K014038.

Who is the listed applicant for PYLORITEK VP TEST KIT 5140VP?

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

What is the FDA product code for PYLORITEK VP TEST KIT 5140VP?

The FDA product code for PYLORITEK VP TEST KIT 5140VP is LYR.

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 Serim Research 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 27 devices →

Related Devices (Code: LYR)

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.

↑