NO. 86500 - ENDOSCOPIC JET WASHER
K-Number: K892426 · 1989-06-22
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Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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