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FDA 510(k)

GALILEO DISPOSABLE HYSTEROSCOPES

K-Number: K981828 · 1998-07-07

Decision Date1998-07-07
Product CodeHIH
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

GALILEO DISPOSABLE HYSTEROSCOPES is the device name listed in this FDA 510(k) record. The listed applicant is Netoptix Corp.. It received FDA 510(k) clearance on 1998-07-07 under 510(k) number K981828. The device is classified under product code HIH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GALILEO DISPOSABLE HYSTEROSCOPES?

GALILEO DISPOSABLE HYSTEROSCOPES is a medical device that received FDA 510(k) clearance on 1998-07-07. The listed applicant is Netoptix Corp.. The 510(k) number is K981828.

When did GALILEO DISPOSABLE HYSTEROSCOPES receive FDA 510(k) clearance?

GALILEO DISPOSABLE HYSTEROSCOPES received FDA 510(k) clearance on 1998-07-07, under 510(k) number K981828.

Who is the listed applicant for GALILEO DISPOSABLE HYSTEROSCOPES?

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

What is the FDA product code for GALILEO DISPOSABLE HYSTEROSCOPES?

The FDA product code for GALILEO DISPOSABLE HYSTEROSCOPES is HIH.

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 Netoptix Corp. 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: HIH)

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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