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FDA 510(k)

RAMP RAT

K-Number: K911986 · 1991-05-31

ApplicantVehicle Dynamics
Decision Date1991-05-31
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

RAMP RAT is the device name listed in this FDA 510(k) record. The listed applicant is Vehicle Dynamics. It received FDA 510(k) clearance on 1991-05-31 under 510(k) number K911986. 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 RAMP RAT?

RAMP RAT is a medical device that received FDA 510(k) clearance on 1991-05-31. The listed applicant is Vehicle Dynamics. The 510(k) number is K911986.

When did RAMP RAT receive FDA 510(k) clearance?

RAMP RAT received FDA 510(k) clearance on 1991-05-31, under 510(k) number K911986.

Who is the listed applicant for RAMP RAT?

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

What is the FDA product code for RAMP RAT?

The FDA product code for RAMP RAT is ITI.

Related Devices (Code: ITI)

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.

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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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