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FDA 510(k)

LOCAL PLEXUS BLOCK ANESTHESIA CATHETER KITS

K-Number: K904440 · 1991-06-07

Decision Date1991-06-07
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LOCAL PLEXUS BLOCK ANESTHESIA CATHETER KITS is the device name listed in this FDA 510(k) record. The listed applicant is Preferred Medical Products. It received FDA 510(k) clearance on 1991-06-07 under 510(k) number K904440. 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 LOCAL PLEXUS BLOCK ANESTHESIA CATHETER KITS?

LOCAL PLEXUS BLOCK ANESTHESIA CATHETER KITS is a medical device that received FDA 510(k) clearance on 1991-06-07. The listed applicant is Preferred Medical Products. The 510(k) number is K904440.

When did LOCAL PLEXUS BLOCK ANESTHESIA CATHETER KITS receive FDA 510(k) clearance?

LOCAL PLEXUS BLOCK ANESTHESIA CATHETER KITS received FDA 510(k) clearance on 1991-06-07, under 510(k) number K904440.

Who is the listed applicant for LOCAL PLEXUS BLOCK ANESTHESIA CATHETER KITS?

The FDA 510(k) record lists Preferred Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LOCAL PLEXUS BLOCK ANESTHESIA CATHETER KITS?

The FDA product code for LOCAL PLEXUS BLOCK ANESTHESIA CATHETER KITS 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 Preferred Medical Products 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

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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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