LD GENERAL PURPOSE DISINFECTANT
K-Number: K952929 · 1995-10-07
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Device Summary
Frequently Asked Questions
What is the LD GENERAL PURPOSE DISINFECTANT?
LD GENERAL PURPOSE DISINFECTANT is a medical device that received FDA 510(k) clearance on 1995-10-07. The listed applicant is Alcide Corp.. The 510(k) number is K952929.
When did LD GENERAL PURPOSE DISINFECTANT receive FDA 510(k) clearance?
LD GENERAL PURPOSE DISINFECTANT received FDA 510(k) clearance on 1995-10-07, under 510(k) number K952929.
Who is the listed applicant for LD GENERAL PURPOSE DISINFECTANT?
The FDA 510(k) record lists Alcide Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LD GENERAL PURPOSE DISINFECTANT?
The FDA product code for LD GENERAL PURPOSE DISINFECTANT is LRJ. This falls under the Clinical Lab category.
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 Alcide 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.
Related Devices (Code: LRJ)
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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