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FDA 510(k)

MASON EQUIPMENT ORGANIZER & ASPEN

K-Number: K843801 · 1984-10-25

Decision Date1984-10-25
Product CodeFSE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MASON EQUIPMENT ORGANIZER & ASPEN is the device name listed in this FDA 510(k) record. The listed applicant is Aspen Laboratories, Inc.. It received FDA 510(k) clearance on 1984-10-25 under 510(k) number K843801. The device is classified under product code FSE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MASON EQUIPMENT ORGANIZER & ASPEN?

MASON EQUIPMENT ORGANIZER & ASPEN is a medical device that received FDA 510(k) clearance on 1984-10-25. The listed applicant is Aspen Laboratories, Inc.. The 510(k) number is K843801.

When did MASON EQUIPMENT ORGANIZER & ASPEN receive FDA 510(k) clearance?

MASON EQUIPMENT ORGANIZER & ASPEN received FDA 510(k) clearance on 1984-10-25, under 510(k) number K843801.

Who is the listed applicant for MASON EQUIPMENT ORGANIZER & ASPEN?

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

What is the FDA product code for MASON EQUIPMENT ORGANIZER & ASPEN?

The FDA product code for MASON EQUIPMENT ORGANIZER & ASPEN is FSE.

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 Aspen Laboratories, 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.

View all 55 devices →

Related Devices (Code: FSE)

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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