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FDA 510(k)

VIEW READING STATION

K-Number: K003688 · 2001-01-22

Decision Date2001-01-22
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VIEW READING STATION is the device name listed in this FDA 510(k) record. The listed applicant is Electromed Intl., Ltd.. It received FDA 510(k) clearance on 2001-01-22 under 510(k) number K003688. 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 VIEW READING STATION?

VIEW READING STATION is a medical device that received FDA 510(k) clearance on 2001-01-22. The listed applicant is Electromed Intl., Ltd.. The 510(k) number is K003688.

When did VIEW READING STATION receive FDA 510(k) clearance?

VIEW READING STATION received FDA 510(k) clearance on 2001-01-22, under 510(k) number K003688.

Who is the listed applicant for VIEW READING STATION?

The FDA 510(k) record lists Electromed Intl., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VIEW READING STATION?

The FDA product code for VIEW READING STATION 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 Electromed Intl., Ltd. 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 23 devices →

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.

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