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FDA 510(k)

10.0MM SUCTION/IRRIGATION PROBE & TUBING KIT

K-Number: K932762 · 1993-08-31

Decision Date1993-08-31
Product CodeGCS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

10.0MM SUCTION/IRRIGATION PROBE & TUBING KIT is the device name listed in this FDA 510(k) record. The listed applicant is Inman Medical Corp.. It received FDA 510(k) clearance on 1993-08-31 under 510(k) number K932762. The device is classified under product code GCS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 10.0MM SUCTION/IRRIGATION PROBE & TUBING KIT?

10.0MM SUCTION/IRRIGATION PROBE & TUBING KIT is a medical device that received FDA 510(k) clearance on 1993-08-31. The listed applicant is Inman Medical Corp.. The 510(k) number is K932762.

When did 10.0MM SUCTION/IRRIGATION PROBE & TUBING KIT receive FDA 510(k) clearance?

10.0MM SUCTION/IRRIGATION PROBE & TUBING KIT received FDA 510(k) clearance on 1993-08-31, under 510(k) number K932762.

Who is the listed applicant for 10.0MM SUCTION/IRRIGATION PROBE & TUBING KIT?

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

What is the FDA product code for 10.0MM SUCTION/IRRIGATION PROBE & TUBING KIT?

The FDA product code for 10.0MM SUCTION/IRRIGATION PROBE & TUBING KIT is GCS.

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 Inman Medical 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.

View all 14 devices →

Related Devices (Code: GCS)

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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