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FDA 510(k)

ULTRASONIC TIPS

K-Number: K812126 · 1981-09-18

ApplicantCooperVision, Inc.
Decision Date1981-09-18
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ULTRASONIC TIPS is the device name listed in this FDA 510(k) record. The listed applicant is CooperVision, Inc.. It received FDA 510(k) clearance on 1981-09-18 under 510(k) number K812126. The device is classified under product code HQC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRASONIC TIPS?

ULTRASONIC TIPS is a medical device that received FDA 510(k) clearance on 1981-09-18. The listed applicant is CooperVision, Inc.. The 510(k) number is K812126.

When did ULTRASONIC TIPS receive FDA 510(k) clearance?

ULTRASONIC TIPS received FDA 510(k) clearance on 1981-09-18, under 510(k) number K812126.

Who is the listed applicant for ULTRASONIC TIPS?

The FDA 510(k) record lists CooperVision, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ULTRASONIC TIPS?

The FDA product code for ULTRASONIC TIPS is HQC.

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Related Devices (Code: HQC)

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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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