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FDA 510(k)

EPIDURAL ANESTHESIA KIT AND COMBINED SPINAL EPIDURAL ANESTHESIA KIT

K-Number: K962821 · 1996-11-13

Decision Date1996-11-13
Product CodeCAZ
Advisory CommitteeAN
DecisionUnknown

Device Summary

EPIDURAL ANESTHESIA KIT AND COMBINED SPINAL EPIDURAL ANESTHESIA KIT is the device name listed in this FDA 510(k) record. The listed applicant is Global Medical Products, Ltd.. It received FDA 510(k) clearance on 1996-11-13 under 510(k) number K962821. 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 EPIDURAL ANESTHESIA KIT AND COMBINED SPINAL EPIDURAL ANESTHESIA KIT?

EPIDURAL ANESTHESIA KIT AND COMBINED SPINAL EPIDURAL ANESTHESIA KIT is a medical device that received FDA 510(k) clearance on 1996-11-13. The listed applicant is Global Medical Products, Ltd.. The 510(k) number is K962821.

When did EPIDURAL ANESTHESIA KIT AND COMBINED SPINAL EPIDURAL ANESTHESIA KIT receive FDA 510(k) clearance?

EPIDURAL ANESTHESIA KIT AND COMBINED SPINAL EPIDURAL ANESTHESIA KIT received FDA 510(k) clearance on 1996-11-13, under 510(k) number K962821.

Who is the listed applicant for EPIDURAL ANESTHESIA KIT AND COMBINED SPINAL EPIDURAL ANESTHESIA KIT?

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

What is the FDA product code for EPIDURAL ANESTHESIA KIT AND COMBINED SPINAL EPIDURAL ANESTHESIA KIT?

The FDA product code for EPIDURAL ANESTHESIA KIT AND COMBINED SPINAL EPIDURAL ANESTHESIA 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 Global Medical Products, Ltd. 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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