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FDA 510(k)

MIDAS REX OPERATING ROOM VISE

K-Number: K854123 · 1985-11-13

ApplicantMidas Rex Pneumatic Tools, Inc.
Decision Date1985-11-13
Product Code
DecisionSubstantially Equivalent

Device Summary

MIDAS REX OPERATING ROOM VISE 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 1985-11-13 under 510(k) number K854123. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIDAS REX OPERATING ROOM VISE?

MIDAS REX OPERATING ROOM VISE is a medical device that received FDA 510(k) clearance on 1985-11-13. The listed applicant is Midas Rex Pneumatic Tools, Inc.. The 510(k) number is K854123.

When did MIDAS REX OPERATING ROOM VISE receive FDA 510(k) clearance?

MIDAS REX OPERATING ROOM VISE received FDA 510(k) clearance on 1985-11-13, under 510(k) number K854123.

Who is the listed applicant for MIDAS REX OPERATING ROOM VISE?

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

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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.

K972289MIDAS REX MOTORK970965MIDAS REX III MOTOR AND ATTACHMENTS (MIDAS III)K962483MIDAS REX III MOTORK953434MIDAS REX MOTORS, (MIDAS I, MIDAS II & CONVERTIBLE MODELS)K954076MIDAS REX DRILL ATTACHMENTS & TWIST DRILLSK953433MIDAS REX TELESCOPING SYSTEM

View all 12 devices →

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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