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FDA 510(k)

APEX MEDICAL MININEB & MINIPLUS

K-Number: K050104 · 2005-02-16

ApplicantApex Medical Corp.
Decision Date2005-02-16
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

APEX MEDICAL MININEB & MINIPLUS is the device name listed in this FDA 510(k) record. The listed applicant is Apex Medical Corp.. It received FDA 510(k) clearance on 2005-02-16 under 510(k) number K050104. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the APEX MEDICAL MININEB & MINIPLUS?

APEX MEDICAL MININEB & MINIPLUS is a medical device that received FDA 510(k) clearance on 2005-02-16. The listed applicant is Apex Medical Corp.. The 510(k) number is K050104.

When did APEX MEDICAL MININEB & MINIPLUS receive FDA 510(k) clearance?

APEX MEDICAL MININEB & MINIPLUS received FDA 510(k) clearance on 2005-02-16, under 510(k) number K050104.

Who is the listed applicant for APEX MEDICAL MININEB & MINIPLUS?

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

What is the FDA product code for APEX MEDICAL MININEB & MINIPLUS?

The FDA product code for APEX MEDICAL MININEB & MINIPLUS is CAF.

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Other records listing Apex Medical Corp. as applicant

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Related Devices (Code: CAF)

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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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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