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FDA 510(k)

CONTINUOUS EPIDURAL ANESTHESIA TRAY

K-Number: K781052 · 1978-08-02

ApplicantPortex, Inc.
Decision Date1978-08-02
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CONTINUOUS EPIDURAL ANESTHESIA TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Portex, Inc.. It received FDA 510(k) clearance on 1978-08-02 under 510(k) number K781052. 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 CONTINUOUS EPIDURAL ANESTHESIA TRAY?

CONTINUOUS EPIDURAL ANESTHESIA TRAY is a medical device that received FDA 510(k) clearance on 1978-08-02. The listed applicant is Portex, Inc.. The 510(k) number is K781052.

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

CONTINUOUS EPIDURAL ANESTHESIA TRAY received FDA 510(k) clearance on 1978-08-02, under 510(k) number K781052.

Who is the listed applicant for CONTINUOUS EPIDURAL ANESTHESIA TRAY?

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

What is the FDA product code for CONTINUOUS EPIDURAL ANESTHESIA TRAY?

The FDA product code for CONTINUOUS EPIDURAL ANESTHESIA TRAY is CAZ.

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Other records listing Portex, 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.

K033080PORTEX 24G PEDIATRIC EPIDURAL AND PERIPHERAL BLOCK ANESTHESIA CATHETERK031057PER-FIT PERCUTANEOUS DILATIONAL TRACHEOSTOMY KITK0237931ST RESPONSE INTERMEDIATE MANUAL RESUSCITATORK0141151ST RESPONSE MANUAL RESUSCITATOR, MODEL 85XXK014073HYPODERMIC NEEDLE-PRO INSULIN SYRINE & NEEDLE WITH NEEDLE PROTECTION DEVICEK873992LARYNGECTOMY TUBE

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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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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