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FDA 510(k)

LARES RESEARCH AS-1 LOWSPEED HANDPIECE

K-Number: K961163 · 1996-04-23

Decision Date1996-04-23
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LARES RESEARCH AS-1 LOWSPEED HANDPIECE 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 1996-04-23 under 510(k) number K961163. 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 RESEARCH AS-1 LOWSPEED HANDPIECE?

LARES RESEARCH AS-1 LOWSPEED HANDPIECE is a medical device that received FDA 510(k) clearance on 1996-04-23. The listed applicant is Lares Research, Inc.. The 510(k) number is K961163.

When did LARES RESEARCH AS-1 LOWSPEED HANDPIECE receive FDA 510(k) clearance?

LARES RESEARCH AS-1 LOWSPEED HANDPIECE received FDA 510(k) clearance on 1996-04-23, under 510(k) number K961163.

Who is the listed applicant for LARES RESEARCH AS-1 LOWSPEED HANDPIECE?

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 RESEARCH AS-1 LOWSPEED HANDPIECE?

The FDA product code for LARES RESEARCH AS-1 LOWSPEED HANDPIECE 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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