FREEDOM LINE LUBRICATED MODELS LS-2-5, LT-6-10
K-Number: K852816 · 1985-10-24
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Device Summary
Frequently Asked Questions
What is the FREEDOM LINE LUBRICATED MODELS LS-2-5, LT-6-10?
FREEDOM LINE LUBRICATED MODELS LS-2-5, LT-6-10 is a medical device that received FDA 510(k) clearance on 1985-10-24. The listed applicant is Apollo Dental Products, Inc.. The 510(k) number is K852816.
When did FREEDOM LINE LUBRICATED MODELS LS-2-5, LT-6-10 receive FDA 510(k) clearance?
FREEDOM LINE LUBRICATED MODELS LS-2-5, LT-6-10 received FDA 510(k) clearance on 1985-10-24, under 510(k) number K852816.
Who is the listed applicant for FREEDOM LINE LUBRICATED MODELS LS-2-5, LT-6-10?
The FDA 510(k) record lists Apollo Dental Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FREEDOM LINE LUBRICATED MODELS LS-2-5, LT-6-10?
The FDA product code for FREEDOM LINE LUBRICATED MODELS LS-2-5, LT-6-10 is EIA.
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 Apollo Dental Products, 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: EIA)
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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