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FDA 510(k)

EURO TECH MARQUISE CHIROPRACTIC TABLE

K-Number: K943974 · 1994-09-29

Decision Date1994-09-29
Product CodeINW
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

EURO TECH MARQUISE CHIROPRACTIC TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Progressive Electrical Therapeutics. It received FDA 510(k) clearance on 1994-09-29 under 510(k) number K943974. The device is classified under product code INW. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EURO TECH MARQUISE CHIROPRACTIC TABLE?

EURO TECH MARQUISE CHIROPRACTIC TABLE is a medical device that received FDA 510(k) clearance on 1994-09-29. The listed applicant is Progressive Electrical Therapeutics. The 510(k) number is K943974.

When did EURO TECH MARQUISE CHIROPRACTIC TABLE receive FDA 510(k) clearance?

EURO TECH MARQUISE CHIROPRACTIC TABLE received FDA 510(k) clearance on 1994-09-29, under 510(k) number K943974.

Who is the listed applicant for EURO TECH MARQUISE CHIROPRACTIC TABLE?

The FDA 510(k) record lists Progressive Electrical Therapeutics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EURO TECH MARQUISE CHIROPRACTIC TABLE?

The FDA product code for EURO TECH MARQUISE CHIROPRACTIC TABLE is INW.

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 Progressive Electrical Therapeutics 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 10 devices →

Related Devices (Code: INW)

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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