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FDA 510(k)

LARES APOLLO CS AND S HANDPIECE LIGHTING SYSTEMS

K-Number: K905542 · 1991-03-11

Decision Date1991-03-11
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LARES APOLLO CS AND S HANDPIECE LIGHTING SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Lares Research, Inc.. It received FDA 510(k) clearance on 1991-03-11 under 510(k) number K905542. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LARES APOLLO CS AND S HANDPIECE LIGHTING SYSTEMS?

LARES APOLLO CS AND S HANDPIECE LIGHTING SYSTEMS is a medical device that received FDA 510(k) clearance on 1991-03-11. The listed applicant is Lares Research, Inc.. The 510(k) number is K905542.

When did LARES APOLLO CS AND S HANDPIECE LIGHTING SYSTEMS receive FDA 510(k) clearance?

LARES APOLLO CS AND S HANDPIECE LIGHTING SYSTEMS received FDA 510(k) clearance on 1991-03-11, under 510(k) number K905542.

Who is the listed applicant for LARES APOLLO CS AND S HANDPIECE LIGHTING SYSTEMS?

The FDA 510(k) record lists Lares Research, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LARES APOLLO CS AND S HANDPIECE LIGHTING SYSTEMS?

The FDA product code for LARES APOLLO CS AND S HANDPIECE LIGHTING SYSTEMS is EFB.

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 Lares Research, 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.

View all 7 devices →

Related Devices (Code: EFB)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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