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FDA 510(k)

AUTOMATED HYDROSONICS(TM)

K-Number: K902798 · 1990-08-28

Decision Date1990-08-28
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

AUTOMATED HYDROSONICS(TM) is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Surgical, Inc.. It received FDA 510(k) clearance on 1990-08-28 under 510(k) number K902798. 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 AUTOMATED HYDROSONICS(TM)?

AUTOMATED HYDROSONICS(TM) is a medical device that received FDA 510(k) clearance on 1990-08-28. The listed applicant is Alcon Surgical, Inc.. The 510(k) number is K902798.

When did AUTOMATED HYDROSONICS(TM) receive FDA 510(k) clearance?

AUTOMATED HYDROSONICS(TM) received FDA 510(k) clearance on 1990-08-28, under 510(k) number K902798.

Who is the listed applicant for AUTOMATED HYDROSONICS(TM)?

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

What is the FDA product code for AUTOMATED HYDROSONICS(TM)?

The FDA product code for AUTOMATED HYDROSONICS(TM) is HQC.

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.

Other records listing Alcon Surgical, Inc. 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: HQC)

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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