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FDA 510(k)

MEDICAL ALERT SYSTEM, MODEL 2200 & 4400 V/T

K-Number: K904796 · 1990-11-26

ApplicantPersonal Emergency Response System
Decision Date1990-11-26
Product CodeILQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MEDICAL ALERT SYSTEM, MODEL 2200 & 4400 V/T is the device name listed in this FDA 510(k) record. The listed applicant is Personal Emergency Response System. It received FDA 510(k) clearance on 1990-11-26 under 510(k) number K904796. 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 MEDICAL ALERT SYSTEM, MODEL 2200 & 4400 V/T?

MEDICAL ALERT SYSTEM, MODEL 2200 & 4400 V/T is a medical device that received FDA 510(k) clearance on 1990-11-26. The listed applicant is Personal Emergency Response System. The 510(k) number is K904796.

When did MEDICAL ALERT SYSTEM, MODEL 2200 & 4400 V/T receive FDA 510(k) clearance?

MEDICAL ALERT SYSTEM, MODEL 2200 & 4400 V/T received FDA 510(k) clearance on 1990-11-26, under 510(k) number K904796.

Who is the listed applicant for MEDICAL ALERT SYSTEM, MODEL 2200 & 4400 V/T?

The FDA 510(k) record lists Personal Emergency Response System as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDICAL ALERT SYSTEM, MODEL 2200 & 4400 V/T?

The FDA product code for MEDICAL ALERT SYSTEM, MODEL 2200 & 4400 V/T is ILQ.

Related Clinical Trials

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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

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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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