FDA 510(k)

IOCARE ULTRASONIC TITANIUM TIPS

K-Number: K843278 · 1984-11-27

Decision Date1984-11-27

Product CodeHQC

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

IOCARE ULTRASONIC TITANIUM TIPS is the device name listed in this FDA 510(k) record. The listed applicant is Chiron Vision Corp.. It received FDA 510(k) clearance on 1984-11-27 under 510(k) number K843278. 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 IOCARE ULTRASONIC TITANIUM TIPS?

IOCARE ULTRASONIC TITANIUM TIPS is a medical device that received FDA 510(k) clearance on 1984-11-27. The listed applicant is Chiron Vision Corp.. The 510(k) number is K843278.

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

IOCARE ULTRASONIC TITANIUM TIPS received FDA 510(k) clearance on 1984-11-27, under 510(k) number K843278.

Who is the listed applicant for IOCARE ULTRASONIC TITANIUM TIPS?

The FDA 510(k) record lists Chiron Vision Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IOCARE ULTRASONIC TITANIUM TIPS?

The FDA product code for IOCARE ULTRASONIC TITANIUM TIPS is HQC.

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Related Devices (Code: HQC)

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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.