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FDA 510(k)

ULTIMA CHIROPRACTIC TABLES

K-Number: K843877 · 1984-11-27

Decision Date1984-11-27
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ULTIMA CHIROPRACTIC TABLES is the device name listed in this FDA 510(k) record. The listed applicant is Elenex Medequip, Inc.. It received FDA 510(k) clearance on 1984-11-27 under 510(k) number K843877. The device is classified under product code INQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTIMA CHIROPRACTIC TABLES?

ULTIMA CHIROPRACTIC TABLES is a medical device that received FDA 510(k) clearance on 1984-11-27. The listed applicant is Elenex Medequip, Inc.. The 510(k) number is K843877.

When did ULTIMA CHIROPRACTIC TABLES receive FDA 510(k) clearance?

ULTIMA CHIROPRACTIC TABLES received FDA 510(k) clearance on 1984-11-27, under 510(k) number K843877.

Who is the listed applicant for ULTIMA CHIROPRACTIC TABLES?

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

What is the FDA product code for ULTIMA CHIROPRACTIC TABLES?

The FDA product code for ULTIMA CHIROPRACTIC TABLES is INQ.

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.

Related Devices (Code: INQ)

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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