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FDA 510(k)

EPIDURAL ANESTHESIA TRAY

K-Number: K885278 · 1989-03-16

ApplicantPreferred Medical Products
Decision Date1989-03-16
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EPIDURAL 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 1989-03-16 under 510(k) number K885278. 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 ANESTHESIA TRAY?

EPIDURAL ANESTHESIA TRAY is a medical device that received FDA 510(k) clearance on 1989-03-16. The listed applicant is Preferred Medical Products. The 510(k) number is K885278.

When did EPIDURAL ANESTHESIA TRAY receive FDA 510(k) clearance?

EPIDURAL ANESTHESIA TRAY received FDA 510(k) clearance on 1989-03-16, under 510(k) number K885278.

Who is the listed applicant for EPIDURAL 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 EPIDURAL ANESTHESIA TRAY?

The FDA product code for EPIDURAL 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.

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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.

K941153EPI-SPINAL ANESTHESIA TRAYK924699PMP MUSCLE STIMULATORK920808OB/GYN DRAPEK904440LOCAL PLEXUS BLOCK ANESTHESIA CATHETER KITSK885277SPINAL ANESTHESIA TRAY

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.

K261372Profoject™ LOR SyringeCMT Health PTE., Ltd.K222341Arrow 0.2 Micron Flat Filter, GVSArrow International, LLCK210983BD Epilor SyringeBecton, Dickinson and CompanyK201356Plastic LOR SyringeJiangsu Caina Medical Co.,LtdK202699E-Cath STIM acc. TsuiPAJUNK GmbH MedizintechnologieK190345VPCPAJUNK GmbH Medizintechnologie

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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