DESERET LONG TERM INDWELLING CATHETER
K-Number: K840958 · 1984-04-17
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Device Summary
Frequently Asked Questions
What is the DESERET LONG TERM INDWELLING CATHETER?
DESERET LONG TERM INDWELLING CATHETER is a medical device that received FDA 510(k) clearance on 1984-04-17. The listed applicant is Parke-Davis Co.. The 510(k) number is K840958.
When did DESERET LONG TERM INDWELLING CATHETER receive FDA 510(k) clearance?
DESERET LONG TERM INDWELLING CATHETER received FDA 510(k) clearance on 1984-04-17, under 510(k) number K840958.
Who is the listed applicant for DESERET LONG TERM INDWELLING CATHETER?
The FDA 510(k) record lists Parke-Davis Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DESERET LONG TERM INDWELLING CATHETER?
The FDA product code for DESERET LONG TERM INDWELLING CATHETER is LJS.
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 Parke-Davis Co. 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: LJS)
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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