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FDA 510(k)

TOUCH TALKER

K-Number: K914259 · 1992-02-27

ApplicantPrentke Romich Co.
Decision Date1992-02-27
Product CodeILQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TOUCH TALKER is the device name listed in this FDA 510(k) record. The listed applicant is Prentke Romich Co.. It received FDA 510(k) clearance on 1992-02-27 under 510(k) number K914259. The device is classified under product code ILQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOUCH TALKER?

TOUCH TALKER is a medical device that received FDA 510(k) clearance on 1992-02-27. The listed applicant is Prentke Romich Co.. The 510(k) number is K914259.

When did TOUCH TALKER receive FDA 510(k) clearance?

TOUCH TALKER received FDA 510(k) clearance on 1992-02-27, under 510(k) number K914259.

Who is the listed applicant for TOUCH TALKER?

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

What is the FDA product code for TOUCH TALKER?

The FDA product code for TOUCH TALKER is ILQ.

Related Clinical Trials

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Other records listing Prentke Romich Co. as applicant

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.

K961306DELTATALKER WITH INFRAREDK944585SCANNING DIRECTORK935317ALPHA TALKERK933207WALKERTALKERK925387LIBERATORK925527LIGHT TALKER

View all 9 devices →

Related Devices (Code: ILQ)

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.

K162817Noddle(TM)Iowa Adaptive Technologies, Inc. Dba Voxello, Inc.K943035P.A.T. SYSTEMMathews Assoc., Inc.K930044COMFORT KEYBOARD SYSTEMHealth Care Keyboard Co., Inc.K931855LIGHTWRITERZygo Corp.K935244R & D BATTERIES, INC. PART NUMBER 5113R & D Batteries, Inc.K935981MLT-2Med Labs, Inc.

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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