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FDA 510(k)

MIDAS REX III MOTOR

K-Number: K962483 · 1996-11-19

Decision Date1996-11-19
Product CodeHBB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MIDAS REX III MOTOR is the device name listed in this FDA 510(k) record. The listed applicant is Midas Rex Pneumatic Tools, Inc.. It received FDA 510(k) clearance on 1996-11-19 under 510(k) number K962483. The device is classified under product code HBB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIDAS REX III MOTOR?

MIDAS REX III MOTOR is a medical device that received FDA 510(k) clearance on 1996-11-19. The listed applicant is Midas Rex Pneumatic Tools, Inc.. The 510(k) number is K962483.

When did MIDAS REX III MOTOR receive FDA 510(k) clearance?

MIDAS REX III MOTOR received FDA 510(k) clearance on 1996-11-19, under 510(k) number K962483.

Who is the listed applicant for MIDAS REX III MOTOR?

The FDA 510(k) record lists Midas Rex Pneumatic Tools, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MIDAS REX III MOTOR?

The FDA product code for MIDAS REX III MOTOR is HBB.

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 Midas Rex Pneumatic Tools, 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 12 devices →

Related Devices (Code: HBB)

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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