MIDAS REX MOTORS (MIDAS I, II & CONVERTIBLE MODELS)
K-Number: K952300 · 1995-05-26
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Device Summary
Frequently Asked Questions
What is the MIDAS REX MOTORS (MIDAS I, II & CONVERTIBLE MODELS)?
MIDAS REX MOTORS (MIDAS I, II & CONVERTIBLE MODELS) is a medical device that received FDA 510(k) clearance on 1995-05-26. The listed applicant is Midas Rex Pneumatic Tools, Inc.. The 510(k) number is K952300.
When did MIDAS REX MOTORS (MIDAS I, II & CONVERTIBLE MODELS) receive FDA 510(k) clearance?
MIDAS REX MOTORS (MIDAS I, II & CONVERTIBLE MODELS) received FDA 510(k) clearance on 1995-05-26, under 510(k) number K952300.
Who is the listed applicant for MIDAS REX MOTORS (MIDAS I, II & CONVERTIBLE MODELS)?
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 MOTORS (MIDAS I, II & CONVERTIBLE MODELS)?
The FDA product code for MIDAS REX MOTORS (MIDAS I, II & CONVERTIBLE MODELS) is GET.
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.
Related Devices (Code: GET)
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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