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FDA 510(k)

BIO MEDX AIR FLOTATION SYSTEM

K-Number: K905156 · 1990-11-27

Decision Date1990-11-27
Product CodeIOQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BIO MEDX AIR FLOTATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Bio Clinic Co.. It received FDA 510(k) clearance on 1990-11-27 under 510(k) number K905156. The device is classified under product code IOQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIO MEDX AIR FLOTATION SYSTEM?

BIO MEDX AIR FLOTATION SYSTEM is a medical device that received FDA 510(k) clearance on 1990-11-27. The listed applicant is Bio Clinic Co.. The 510(k) number is K905156.

When did BIO MEDX AIR FLOTATION SYSTEM receive FDA 510(k) clearance?

BIO MEDX AIR FLOTATION SYSTEM received FDA 510(k) clearance on 1990-11-27, under 510(k) number K905156.

Who is the listed applicant for BIO MEDX AIR FLOTATION SYSTEM?

The FDA 510(k) record lists Bio Clinic Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIO MEDX AIR FLOTATION SYSTEM?

The FDA product code for BIO MEDX AIR FLOTATION SYSTEM is IOQ.

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 Bio Clinic Co. 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 14 devices →

Related Devices (Code: IOQ)

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

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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