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FDA 510(k)

SUCTION AND IRRIGATION TUBES

K-Number: K942202 · 1994-05-25

Decision Date1994-05-25
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SUCTION AND IRRIGATION TUBES is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corp.. It received FDA 510(k) clearance on 1994-05-25 under 510(k) number K942202. 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 SUCTION AND IRRIGATION TUBES?

SUCTION AND IRRIGATION TUBES is a medical device that received FDA 510(k) clearance on 1994-05-25. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K942202.

When did SUCTION AND IRRIGATION TUBES receive FDA 510(k) clearance?

SUCTION AND IRRIGATION TUBES received FDA 510(k) clearance on 1994-05-25, under 510(k) number K942202.

Who is the listed applicant for SUCTION AND IRRIGATION TUBES?

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

What is the FDA product code for SUCTION AND IRRIGATION TUBES?

The FDA product code for SUCTION AND IRRIGATION TUBES 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 Richard Wolf Medical Instruments 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 142 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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