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FDA 510(k)

NO. 86500 - ENDOSCOPIC JET WASHER

K-Number: K892426 · 1989-06-22

Decision Date1989-06-22
Product CodeOCX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NO. 86500 - ENDOSCOPIC JET WASHER is the device name listed in this FDA 510(k) record. The listed applicant is Superior Healthcare Group, Inc.. It received FDA 510(k) clearance on 1989-06-22 under 510(k) number K892426. The device is classified under product code OCX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NO. 86500 - ENDOSCOPIC JET WASHER?

NO. 86500 - ENDOSCOPIC JET WASHER is a medical device that received FDA 510(k) clearance on 1989-06-22. The listed applicant is Superior Healthcare Group, Inc.. The 510(k) number is K892426.

When did NO. 86500 - ENDOSCOPIC JET WASHER receive FDA 510(k) clearance?

NO. 86500 - ENDOSCOPIC JET WASHER received FDA 510(k) clearance on 1989-06-22, under 510(k) number K892426.

Who is the listed applicant for NO. 86500 - ENDOSCOPIC JET WASHER?

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

What is the FDA product code for NO. 86500 - ENDOSCOPIC JET WASHER?

The FDA product code for NO. 86500 - ENDOSCOPIC JET WASHER is OCX.

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 Superior Healthcare Group, 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 14 devices →

Related Devices (Code: OCX)

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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