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FDA 510(k)

APEX DISPOSABLE INSTRUMENTS

K-Number: K941907 · 1994-08-26

ApplicantApex Ent., Inc.
Decision Date1994-08-26
Product CodeMDM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

APEX DISPOSABLE INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Apex Ent., Inc.. It received FDA 510(k) clearance on 1994-08-26 under 510(k) number K941907. The device is classified under product code MDM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the APEX DISPOSABLE INSTRUMENTS?

APEX DISPOSABLE INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1994-08-26. The listed applicant is Apex Ent., Inc.. The 510(k) number is K941907.

When did APEX DISPOSABLE INSTRUMENTS receive FDA 510(k) clearance?

APEX DISPOSABLE INSTRUMENTS received FDA 510(k) clearance on 1994-08-26, under 510(k) number K941907.

Who is the listed applicant for APEX DISPOSABLE INSTRUMENTS?

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

What is the FDA product code for APEX DISPOSABLE INSTRUMENTS?

The FDA product code for APEX DISPOSABLE INSTRUMENTS is MDM.

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Related Devices (Code: MDM)

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

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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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