Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LYNX LOW-SPEED HANDPIECE

K-Number: K900798 · 1990-06-27

Decision Date1990-06-27
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 Air Motors Technologies. It received FDA 510(k) clearance on 1990-06-27 under 510(k) number K900798. 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 1990-06-27. The listed applicant is Air Motors Technologies. The 510(k) number is K900798.

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

LYNX LOW-SPEED HANDPIECE received FDA 510(k) clearance on 1990-06-27, under 510(k) number K900798.

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

The FDA 510(k) record lists Air Motors Technologies 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.

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.

↑