LARES RESEARCH AS-1 LOWSPEED HANDPIECE
K-Number: K961163 · 1996-04-23
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Device Summary
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.
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
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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