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FDA 510(k)

PALL ULTIPOR ANESTHESIA BREATHING SYSTEM

K-Number: K013093 · 2002-08-01

ApplicantPall Medical
Decision Date2002-08-01
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PALL ULTIPOR ANESTHESIA BREATHING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Pall Medical. It received FDA 510(k) clearance on 2002-08-01 under 510(k) number K013093. The device is classified under product code CAH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PALL ULTIPOR ANESTHESIA BREATHING SYSTEM?

PALL ULTIPOR ANESTHESIA BREATHING SYSTEM is a medical device that received FDA 510(k) clearance on 2002-08-01. The listed applicant is Pall Medical. The 510(k) number is K013093.

When did PALL ULTIPOR ANESTHESIA BREATHING SYSTEM receive FDA 510(k) clearance?

PALL ULTIPOR ANESTHESIA BREATHING SYSTEM received FDA 510(k) clearance on 2002-08-01, under 510(k) number K013093.

Who is the listed applicant for PALL ULTIPOR ANESTHESIA BREATHING SYSTEM?

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

What is the FDA product code for PALL ULTIPOR ANESTHESIA BREATHING SYSTEM?

The FDA product code for PALL ULTIPOR ANESTHESIA BREATHING SYSTEM is CAH.

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 Pall Medical 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: CAH)

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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