DESERET EPIDURAL CATHETER
K-Number: K850439 · 1985-03-05
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Device Summary
Frequently Asked Questions
What is the DESERET EPIDURAL CATHETER?
DESERET EPIDURAL CATHETER is a medical device that received FDA 510(k) clearance on 1985-03-05. The listed applicant is Parke-Davis Co.. The 510(k) number is K850439.
When did DESERET EPIDURAL CATHETER receive FDA 510(k) clearance?
DESERET EPIDURAL CATHETER received FDA 510(k) clearance on 1985-03-05, under 510(k) number K850439.
Who is the listed applicant for DESERET EPIDURAL 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 EPIDURAL CATHETER?
The FDA product code for DESERET EPIDURAL CATHETER is BSO.
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: BSO)
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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