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FDA 510(k)

SOFT TIP EPIDURAL CATHETER KIT

K-Number: K971233 · 1997-10-17

Decision Date1997-10-17
Product CodeCAZ
Advisory CommitteeAN
DecisionUnknown

Device Summary

SOFT TIP EPIDURAL CATHETER KIT is the device name listed in this FDA 510(k) record. The listed applicant is B.Braun Medical, Inc.. It received FDA 510(k) clearance on 1997-10-17 under 510(k) number K971233. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the SOFT TIP EPIDURAL CATHETER KIT?

SOFT TIP EPIDURAL CATHETER KIT is a medical device that received FDA 510(k) clearance on 1997-10-17. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K971233.

When did SOFT TIP EPIDURAL CATHETER KIT receive FDA 510(k) clearance?

SOFT TIP EPIDURAL CATHETER KIT received FDA 510(k) clearance on 1997-10-17, under 510(k) number K971233.

Who is the listed applicant for SOFT TIP EPIDURAL CATHETER KIT?

The FDA 510(k) record lists B.Braun Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SOFT TIP EPIDURAL CATHETER KIT?

The FDA product code for SOFT TIP EPIDURAL CATHETER KIT 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 B.Braun Medical, Inc. 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 142 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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