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FDA 510(k)

SPECIALTY CONTROLS INTERFACE

K-Number: K913645 · 1991-12-17

ApplicantEverest & Jennings, Inc.
Decision Date1991-12-17
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SPECIALTY CONTROLS INTERFACE 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 1991-12-17 under 510(k) number K913645. 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 SPECIALTY CONTROLS INTERFACE?

SPECIALTY CONTROLS INTERFACE is a medical device that received FDA 510(k) clearance on 1991-12-17. The listed applicant is Everest & Jennings, Inc.. The 510(k) number is K913645.

When did SPECIALTY CONTROLS INTERFACE receive FDA 510(k) clearance?

SPECIALTY CONTROLS INTERFACE received FDA 510(k) clearance on 1991-12-17, under 510(k) number K913645.

Who is the listed applicant for SPECIALTY CONTROLS INTERFACE?

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 SPECIALTY CONTROLS INTERFACE?

The FDA product code for SPECIALTY CONTROLS INTERFACE 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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