MIDAS REX TELESCOPING SYSTEM
K-Number: K953433 · 1995-09-15
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Device Summary
Frequently Asked Questions
What is the MIDAS REX TELESCOPING SYSTEM?
MIDAS REX TELESCOPING SYSTEM is a medical device that received FDA 510(k) clearance on 1995-09-15. The listed applicant is Midas Rex Pneumatic Tools, Inc.. The 510(k) number is K953433.
When did MIDAS REX TELESCOPING SYSTEM receive FDA 510(k) clearance?
MIDAS REX TELESCOPING SYSTEM received FDA 510(k) clearance on 1995-09-15, under 510(k) number K953433.
Who is the listed applicant for MIDAS REX TELESCOPING SYSTEM?
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 TELESCOPING SYSTEM?
The FDA product code for MIDAS REX TELESCOPING SYSTEM 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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