ALOCLAIR ORAL SPRAY
K-Number: K042722 · 2005-01-13
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Device Summary
Frequently Asked Questions
What is the ALOCLAIR ORAL SPRAY?
ALOCLAIR ORAL SPRAY is a medical device that received FDA 510(k) clearance on 2005-01-13. The listed applicant is Sinclair Pharmaceuticals, Ltd.. The 510(k) number is K042722.
When did ALOCLAIR ORAL SPRAY receive FDA 510(k) clearance?
ALOCLAIR ORAL SPRAY received FDA 510(k) clearance on 2005-01-13, under 510(k) number K042722.
Who is the listed applicant for ALOCLAIR ORAL SPRAY?
The FDA 510(k) record lists Sinclair Pharmaceuticals, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALOCLAIR ORAL SPRAY?
The FDA product code for ALOCLAIR ORAL SPRAY is OLR.
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 Sinclair Pharmaceuticals, 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.
Related Devices (Code: OLR)
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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