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FDA 510(k)

RUNAROUND

K-Number: K862405 · 1986-07-15

ApplicantEverest & Jennings, Inc.
Decision Date1986-07-15
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

RUNAROUND is the device name listed in this FDA 510(k) record. The listed applicant is Everest & Jennings, Inc.. It received FDA 510(k) clearance on 1986-07-15 under 510(k) number K862405. 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 RUNAROUND?

RUNAROUND is a medical device that received FDA 510(k) clearance on 1986-07-15. The listed applicant is Everest & Jennings, Inc.. The 510(k) number is K862405.

When did RUNAROUND receive FDA 510(k) clearance?

RUNAROUND received FDA 510(k) clearance on 1986-07-15, under 510(k) number K862405.

Who is the listed applicant for RUNAROUND?

The FDA 510(k) record lists Everest & Jennings, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RUNAROUND?

The FDA product code for RUNAROUND is ITI.

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Other records listing Everest & Jennings, Inc. as applicant

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Related Devices (Code: ITI)

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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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