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FDA 510(k)

[SPECIALIZED TISSUE ASPIRATING RESECTOSCOPE (STAR)]

K-Number: K962506 · 1996-09-16

Decision Date1996-09-16
Product CodeFJL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

[SPECIALIZED TISSUE ASPIRATING RESECTOSCOPE (STAR)] is the device name listed in this FDA 510(k) record. The listed applicant is Gynecare Innovation Center. It received FDA 510(k) clearance on 1996-09-16 under 510(k) number K962506. The device is classified under product code FJL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the [SPECIALIZED TISSUE ASPIRATING RESECTOSCOPE (STAR)]?

[SPECIALIZED TISSUE ASPIRATING RESECTOSCOPE (STAR)] is a medical device that received FDA 510(k) clearance on 1996-09-16. The listed applicant is Gynecare Innovation Center. The 510(k) number is K962506.

When did [SPECIALIZED TISSUE ASPIRATING RESECTOSCOPE (STAR)] receive FDA 510(k) clearance?

[SPECIALIZED TISSUE ASPIRATING RESECTOSCOPE (STAR)] received FDA 510(k) clearance on 1996-09-16, under 510(k) number K962506.

Who is the listed applicant for [SPECIALIZED TISSUE ASPIRATING RESECTOSCOPE (STAR)]?

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

What is the FDA product code for [SPECIALIZED TISSUE ASPIRATING RESECTOSCOPE (STAR)]?

The FDA product code for [SPECIALIZED TISSUE ASPIRATING RESECTOSCOPE (STAR)] is FJL.

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 Gynecare Innovation Center 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.

View all 8 devices →

Related Devices (Code: FJL)

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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