EPIDURAL CATHETER MODELS 1210/1200
K-Number: K983125 · 1998-11-17
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Device Summary
Frequently Asked Questions
What is the EPIDURAL CATHETER MODELS 1210/1200?
EPIDURAL CATHETER MODELS 1210/1200 is a medical device that received FDA 510(k) clearance on 1998-11-17. The listed applicant is Rusch Intl.. The 510(k) number is K983125.
When did EPIDURAL CATHETER MODELS 1210/1200 receive FDA 510(k) clearance?
EPIDURAL CATHETER MODELS 1210/1200 received FDA 510(k) clearance on 1998-11-17, under 510(k) number K983125.
Who is the listed applicant for EPIDURAL CATHETER MODELS 1210/1200?
The FDA 510(k) record lists Rusch Intl. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EPIDURAL CATHETER MODELS 1210/1200?
The FDA product code for EPIDURAL CATHETER MODELS 1210/1200 is CAZ.
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 Rusch Intl. 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: CAZ)
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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