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FDA 510(k)

EPIDURAL CATHETER MODELS 1210/1200

K-Number: K983125 · 1998-11-17

ApplicantRusch Intl.
Decision Date1998-11-17
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EPIDURAL CATHETER MODELS 1210/1200 is the device name listed in this FDA 510(k) record. The listed applicant is Rusch Intl.. It received FDA 510(k) clearance on 1998-11-17 under 510(k) number K983125. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 43 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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