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)

UNIWEB, VERSION 5.0

K-Number: K071166 · 2007-07-23

Decision Date2007-07-23
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

UNIWEB, VERSION 5.0 is the device name listed in this FDA 510(k) record. The listed applicant is Electronic Business Machine Co., Ltd. (Ebm). It received FDA 510(k) clearance on 2007-07-23 under 510(k) number K071166. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIWEB, VERSION 5.0?

UNIWEB, VERSION 5.0 is a medical device that received FDA 510(k) clearance on 2007-07-23. The listed applicant is Electronic Business Machine Co., Ltd. (Ebm). The 510(k) number is K071166.

When did UNIWEB, VERSION 5.0 receive FDA 510(k) clearance?

UNIWEB, VERSION 5.0 received FDA 510(k) clearance on 2007-07-23, under 510(k) number K071166.

Who is the listed applicant for UNIWEB, VERSION 5.0?

The FDA 510(k) record lists Electronic Business Machine Co., Ltd. (Ebm) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UNIWEB, VERSION 5.0?

The FDA product code for UNIWEB, VERSION 5.0 is LLZ.

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 Electronic Business Machine Co., Ltd. (Ebm) 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: LLZ)

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.

↑