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FDA 510(k)

EZ-MISTER

K-Number: K093584 · 2011-03-04

Decision Date2011-03-04
Product CodeCCT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EZ-MISTER is the device name listed in this FDA 510(k) record. The listed applicant is N.M. Beale Co., Inc.. It received FDA 510(k) clearance on 2011-03-04 under 510(k) number K093584. The device is classified under product code CCT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EZ-MISTER?

EZ-MISTER is a medical device that received FDA 510(k) clearance on 2011-03-04. The listed applicant is N.M. Beale Co., Inc.. The 510(k) number is K093584.

When did EZ-MISTER receive FDA 510(k) clearance?

EZ-MISTER received FDA 510(k) clearance on 2011-03-04, under 510(k) number K093584.

Who is the listed applicant for EZ-MISTER?

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

What is the FDA product code for EZ-MISTER?

The FDA product code for EZ-MISTER is CCT.

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 N.M. Beale Co., 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.

Related Devices (Code: CCT)

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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