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FDA 510(k)

INLET IRRIGATION/ASPIRATION VALVE AND PROBES

K-Number: K923528 · 1993-01-12

ApplicantInlet Medical, Inc.
Decision Date1993-01-12
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

INLET IRRIGATION/ASPIRATION VALVE AND PROBES is the device name listed in this FDA 510(k) record. The listed applicant is Inlet Medical, Inc.. It received FDA 510(k) clearance on 1993-01-12 under 510(k) number K923528. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INLET IRRIGATION/ASPIRATION VALVE AND PROBES?

INLET IRRIGATION/ASPIRATION VALVE AND PROBES is a medical device that received FDA 510(k) clearance on 1993-01-12. The listed applicant is Inlet Medical, Inc.. The 510(k) number is K923528.

When did INLET IRRIGATION/ASPIRATION VALVE AND PROBES receive FDA 510(k) clearance?

INLET IRRIGATION/ASPIRATION VALVE AND PROBES received FDA 510(k) clearance on 1993-01-12, under 510(k) number K923528.

Who is the listed applicant for INLET IRRIGATION/ASPIRATION VALVE AND PROBES?

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

What is the FDA product code for INLET IRRIGATION/ASPIRATION VALVE AND PROBES?

The FDA product code for INLET IRRIGATION/ASPIRATION VALVE AND PROBES is GCJ.

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.

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Other records listing Inlet Medical, 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.

K984600METRA PS PROCEDURE KIT

Related Devices (Code: GCJ)

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.

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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.

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