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FDA 510(k)

EPI-SPINAL ANESTHESIA TRAY

K-Number: K941153 · 1995-05-30

Decision Date1995-05-30
Product CodeCAZ
Advisory CommitteeAN
DecisionUnknown

Device Summary

EPI-SPINAL ANESTHESIA TRAY 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 1995-05-30 under 510(k) number K941153. 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 EPI-SPINAL ANESTHESIA TRAY?

EPI-SPINAL ANESTHESIA TRAY is a medical device that received FDA 510(k) clearance on 1995-05-30. The listed applicant is Preferred Medical Products. The 510(k) number is K941153.

When did EPI-SPINAL ANESTHESIA TRAY receive FDA 510(k) clearance?

EPI-SPINAL ANESTHESIA TRAY received FDA 510(k) clearance on 1995-05-30, under 510(k) number K941153.

Who is the listed applicant for EPI-SPINAL ANESTHESIA TRAY?

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 EPI-SPINAL ANESTHESIA TRAY?

The FDA product code for EPI-SPINAL ANESTHESIA TRAY 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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