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FDA 510(k)

MICOR ANESTHESIA CONDUCTION KIT

K-Number: K001940 · 2000-08-11

ApplicantMicor, Inc.
Decision Date2000-08-11
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MICOR ANESTHESIA CONDUCTION KIT is the device name listed in this FDA 510(k) record. The listed applicant is Micor, Inc.. It received FDA 510(k) clearance on 2000-08-11 under 510(k) number K001940. 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 MICOR ANESTHESIA CONDUCTION KIT?

MICOR ANESTHESIA CONDUCTION KIT is a medical device that received FDA 510(k) clearance on 2000-08-11. The listed applicant is Micor, Inc.. The 510(k) number is K001940.

When did MICOR ANESTHESIA CONDUCTION KIT receive FDA 510(k) clearance?

MICOR ANESTHESIA CONDUCTION KIT received FDA 510(k) clearance on 2000-08-11, under 510(k) number K001940.

Who is the listed applicant for MICOR ANESTHESIA CONDUCTION KIT?

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

What is the FDA product code for MICOR ANESTHESIA CONDUCTION KIT?

The FDA product code for MICOR ANESTHESIA CONDUCTION KIT is CAZ.

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Other records listing Micor, 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.

K031600CONDUCTION CATHETERK003966WUNDCATH CONDUCTION CATHETERK001717MICOR CONDUCTION CATHETERK991879SPRING-WOUND EPIDURAL CATHETERK861008PERCUTANEOUS CATHETERSK860339PERCUTANEOUS CATHETERS

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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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