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FDA 510(k)

TONGUETOUCH KEYPAD AND ZOFCOM CONTROL SYSTEM

K-Number: K911101 · 1991-04-25

ApplicantZofcom, Inc.
Decision Date1991-04-25
Product CodeIQA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TONGUETOUCH KEYPAD AND ZOFCOM CONTROL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Zofcom, Inc.. It received FDA 510(k) clearance on 1991-04-25 under 510(k) number K911101. The device is classified under product code IQA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TONGUETOUCH KEYPAD AND ZOFCOM CONTROL SYSTEM?

TONGUETOUCH KEYPAD AND ZOFCOM CONTROL SYSTEM is a medical device that received FDA 510(k) clearance on 1991-04-25. The listed applicant is Zofcom, Inc.. The 510(k) number is K911101.

When did TONGUETOUCH KEYPAD AND ZOFCOM CONTROL SYSTEM receive FDA 510(k) clearance?

TONGUETOUCH KEYPAD AND ZOFCOM CONTROL SYSTEM received FDA 510(k) clearance on 1991-04-25, under 510(k) number K911101.

Who is the listed applicant for TONGUETOUCH KEYPAD AND ZOFCOM CONTROL SYSTEM?

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

What is the FDA product code for TONGUETOUCH KEYPAD AND ZOFCOM CONTROL SYSTEM?

The FDA product code for TONGUETOUCH KEYPAD AND ZOFCOM CONTROL SYSTEM is IQA.

Related Clinical Trials

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.

Related Devices (Code: IQA)

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.

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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