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FDA 510(k)

EZ-Tip Singles, EZ-Tip Vial of 20, EZ-Grip

K-Number: K161275 · 2017-01-23

Decision Date2017-01-23
Product CodeMQH
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

EZ-Tip Singles, EZ-Tip Vial of 20, EZ-Grip is the device name listed in this FDA 510(k) record. The listed applicant is Research Instruments Limited. It received FDA 510(k) clearance on 2017-01-23 under 510(k) number K161275. The device is classified under product code MQH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EZ-Tip Singles, EZ-Tip Vial of 20, EZ-Grip?

EZ-Tip Singles, EZ-Tip Vial of 20, EZ-Grip is a medical device that received FDA 510(k) clearance on 2017-01-23. The listed applicant is Research Instruments Limited. The 510(k) number is K161275.

When did EZ-Tip Singles, EZ-Tip Vial of 20, EZ-Grip receive FDA 510(k) clearance?

EZ-Tip Singles, EZ-Tip Vial of 20, EZ-Grip received FDA 510(k) clearance on 2017-01-23, under 510(k) number K161275.

Who is the listed applicant for EZ-Tip Singles, EZ-Tip Vial of 20, EZ-Grip?

The FDA 510(k) record lists Research Instruments Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EZ-Tip Singles, EZ-Tip Vial of 20, EZ-Grip?

The FDA product code for EZ-Tip Singles, EZ-Tip Vial of 20, EZ-Grip is MQH.

Other records listing Research Instruments Limited 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: MQH)

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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