Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

FREEDOM LINE LUBRICATED MODELS LS-2-5, LT-6-10

K-Number: K852816 · 1985-10-24

Decision Date1985-10-24
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FREEDOM LINE LUBRICATED MODELS LS-2-5, LT-6-10 is the device name listed in this FDA 510(k) record. The listed applicant is Apollo Dental Products, Inc.. It received FDA 510(k) clearance on 1985-10-24 under 510(k) number K852816. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

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.

↑