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FDA 510(k)

DISPOSABLE ASPIRATION/IRRIGATION TRUMPET VALVE PROBE

K-Number: K941390 · 1994-06-09

Decision Date1994-06-09
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE ASPIRATION/IRRIGATION TRUMPET VALVE PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Deroyal Industries, Inc.. It received FDA 510(k) clearance on 1994-06-09 under 510(k) number K941390. 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 DISPOSABLE ASPIRATION/IRRIGATION TRUMPET VALVE PROBE?

DISPOSABLE ASPIRATION/IRRIGATION TRUMPET VALVE PROBE is a medical device that received FDA 510(k) clearance on 1994-06-09. The listed applicant is Deroyal Industries, Inc.. The 510(k) number is K941390.

When did DISPOSABLE ASPIRATION/IRRIGATION TRUMPET VALVE PROBE receive FDA 510(k) clearance?

DISPOSABLE ASPIRATION/IRRIGATION TRUMPET VALVE PROBE received FDA 510(k) clearance on 1994-06-09, under 510(k) number K941390.

Who is the listed applicant for DISPOSABLE ASPIRATION/IRRIGATION TRUMPET VALVE PROBE?

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

What is the FDA product code for DISPOSABLE ASPIRATION/IRRIGATION TRUMPET VALVE PROBE?

The FDA product code for DISPOSABLE ASPIRATION/IRRIGATION TRUMPET VALVE PROBE 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.

Other records listing Deroyal Industries, 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.

View all 90 devices →

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.

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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