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FDA 510(k)

LCI-100 AND LCI-200 WELCH ALLYN ILLUMINATION AND IMAGING SYSTEM

K-Number: K940270 · 1994-04-20

Decision Date1994-04-20
Product CodeGCT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LCI-100 AND LCI-200 WELCH ALLYN ILLUMINATION AND IMAGING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Welch Allyn, Inc.. It received FDA 510(k) clearance on 1994-04-20 under 510(k) number K940270. The device is classified under product code GCT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LCI-100 AND LCI-200 WELCH ALLYN ILLUMINATION AND IMAGING SYSTEM?

LCI-100 AND LCI-200 WELCH ALLYN ILLUMINATION AND IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 1994-04-20. The listed applicant is Welch Allyn, Inc.. The 510(k) number is K940270.

When did LCI-100 AND LCI-200 WELCH ALLYN ILLUMINATION AND IMAGING SYSTEM receive FDA 510(k) clearance?

LCI-100 AND LCI-200 WELCH ALLYN ILLUMINATION AND IMAGING SYSTEM received FDA 510(k) clearance on 1994-04-20, under 510(k) number K940270.

Who is the listed applicant for LCI-100 AND LCI-200 WELCH ALLYN ILLUMINATION AND IMAGING SYSTEM?

The FDA 510(k) record lists Welch Allyn, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LCI-100 AND LCI-200 WELCH ALLYN ILLUMINATION AND IMAGING SYSTEM?

The FDA product code for LCI-100 AND LCI-200 WELCH ALLYN ILLUMINATION AND IMAGING SYSTEM is GCT.

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 Welch Allyn, Inc. 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 109 devices →

Related Devices (Code: GCT)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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