ENDOSCOPIC ASPIRATION CATHETER SET
K-Number: K844691 · 1985-01-02
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Device Summary
Frequently Asked Questions
What is the ENDOSCOPIC ASPIRATION CATHETER SET?
ENDOSCOPIC ASPIRATION CATHETER SET is a medical device that received FDA 510(k) clearance on 1985-01-02. The listed applicant is Jayco Pharmaceuticals. The 510(k) number is K844691.
When did ENDOSCOPIC ASPIRATION CATHETER SET receive FDA 510(k) clearance?
ENDOSCOPIC ASPIRATION CATHETER SET received FDA 510(k) clearance on 1985-01-02, under 510(k) number K844691.
Who is the listed applicant for ENDOSCOPIC ASPIRATION CATHETER SET?
The FDA 510(k) record lists Jayco Pharmaceuticals as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENDOSCOPIC ASPIRATION CATHETER SET?
The FDA product code for ENDOSCOPIC ASPIRATION CATHETER SET 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 Jayco Pharmaceuticals 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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