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FDA 510(k)

LYNX-SM, SCLAER DENTAL HANDPIECE

K-Number: K901488 · 1990-05-15

ApplicantMti Precision Products
Decision Date1990-05-15
Product CodeELC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LYNX-SM, SCLAER DENTAL 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 1990-05-15 under 510(k) number K901488. The device is classified under product code ELC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LYNX-SM, SCLAER DENTAL HANDPIECE?

LYNX-SM, SCLAER DENTAL HANDPIECE is a medical device that received FDA 510(k) clearance on 1990-05-15. The listed applicant is Mti Precision Products. The 510(k) number is K901488.

When did LYNX-SM, SCLAER DENTAL HANDPIECE receive FDA 510(k) clearance?

LYNX-SM, SCLAER DENTAL HANDPIECE received FDA 510(k) clearance on 1990-05-15, under 510(k) number K901488.

Who is the listed applicant for LYNX-SM, SCLAER DENTAL 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-SM, SCLAER DENTAL HANDPIECE?

The FDA product code for LYNX-SM, SCLAER DENTAL HANDPIECE is ELC.

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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.

K070001MASTER CLASSIC 5K LOW SPEED HANDPIECE, 20K LOW SPEED HANDPIECE, TM5 LOW SPEED HANDPIECE AND TM20 LOW SPEED HANDPIECEK960541LYNX DPA DISPOSABLE PROPHY ANGLEK940261LYNX LOW-SPEED HANDPIECEK895736LYNX-HIGH SPEED HANDPIECE

Related Devices (Code: ELC)

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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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