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FDA 510(k)

LYNX LOW-SPEED HANDPIECE

K-Number: K940261 · 1994-12-29

Decision Date1994-12-29
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LYNX LOW-SPEED HANDPIECE is the device name listed in this FDA 510(k) record. The listed applicant is Mti Precision Products. It received FDA 510(k) clearance on 1994-12-29 under 510(k) number K940261. 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 LYNX LOW-SPEED HANDPIECE?

LYNX LOW-SPEED HANDPIECE is a medical device that received FDA 510(k) clearance on 1994-12-29. The listed applicant is Mti Precision Products. The 510(k) number is K940261.

When did LYNX LOW-SPEED HANDPIECE receive FDA 510(k) clearance?

LYNX LOW-SPEED HANDPIECE received FDA 510(k) clearance on 1994-12-29, under 510(k) number K940261.

Who is the listed applicant for LYNX LOW-SPEED HANDPIECE?

The FDA 510(k) record lists Mti Precision Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LYNX LOW-SPEED HANDPIECE?

The FDA product code for LYNX LOW-SPEED 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 Mti Precision Products 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

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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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