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FDA 510(k)

RTD ARM ASSISTIVE ROBOTIC DEVICE

K-Number: K993443 · 1999-12-17

ApplicantRehabilitation Technologies Division
Decision Date1999-12-17
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

RTD ARM ASSISTIVE ROBOTIC DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Rehabilitation Technologies Division. It received FDA 510(k) clearance on 1999-12-17 under 510(k) number K993443. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RTD ARM ASSISTIVE ROBOTIC DEVICE?

RTD ARM ASSISTIVE ROBOTIC DEVICE is a medical device that received FDA 510(k) clearance on 1999-12-17. The listed applicant is Rehabilitation Technologies Division. The 510(k) number is K993443.

When did RTD ARM ASSISTIVE ROBOTIC DEVICE receive FDA 510(k) clearance?

RTD ARM ASSISTIVE ROBOTIC DEVICE received FDA 510(k) clearance on 1999-12-17, under 510(k) number K993443.

Who is the listed applicant for RTD ARM ASSISTIVE ROBOTIC DEVICE?

The FDA 510(k) record lists Rehabilitation Technologies Division as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RTD ARM ASSISTIVE ROBOTIC DEVICE?

The FDA product code for RTD ARM ASSISTIVE ROBOTIC DEVICE is ITI.

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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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