FDA 510(k)

TURBOSONICS LIMITED REUSE ULTRASONIC TIP

K-Number: K981103 · 1998-06-23

Decision Date1998-06-23

Product CodeHQC

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

TURBOSONICS LIMITED REUSE ULTRASONIC TIP is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Laboratories. It received FDA 510(k) clearance on 1998-06-23 under 510(k) number K981103. 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 TURBOSONICS LIMITED REUSE ULTRASONIC TIP?

TURBOSONICS LIMITED REUSE ULTRASONIC TIP is a medical device that received FDA 510(k) clearance on 1998-06-23. The listed applicant is Alcon Laboratories. The 510(k) number is K981103.

When did TURBOSONICS LIMITED REUSE ULTRASONIC TIP receive FDA 510(k) clearance?

TURBOSONICS LIMITED REUSE ULTRASONIC TIP received FDA 510(k) clearance on 1998-06-23, under 510(k) number K981103.

Who is the listed applicant for TURBOSONICS LIMITED REUSE ULTRASONIC TIP?

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

What is the FDA product code for TURBOSONICS LIMITED REUSE ULTRASONIC TIP?

The FDA product code for TURBOSONICS LIMITED REUSE ULTRASONIC TIP is 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.