LM-150HT LIGHT SOURCE
K-Number: K911212 · 1991-05-23
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Device Summary
Frequently Asked Questions
What is the LM-150HT LIGHT SOURCE?
LM-150HT LIGHT SOURCE is a medical device that received FDA 510(k) clearance on 1991-05-23. The listed applicant is Leisegang Medical, Inc.. The 510(k) number is K911212.
When did LM-150HT LIGHT SOURCE receive FDA 510(k) clearance?
LM-150HT LIGHT SOURCE received FDA 510(k) clearance on 1991-05-23, under 510(k) number K911212.
Who is the listed applicant for LM-150HT LIGHT SOURCE?
The FDA 510(k) record lists Leisegang Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LM-150HT LIGHT SOURCE?
The FDA product code for LM-150HT LIGHT SOURCE is ESI.
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 Leisegang Medical, 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.
Related Devices (Code: ESI)
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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