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FDA 510(k)

LIFELINE(R) PERSONAL RESPONSE SYSTEM

K-Number: K914103 · 1991-09-27

ApplicantLifeline Systems, Inc.
Decision Date1991-09-27
Product CodeILQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LIFELINE(R) PERSONAL RESPONSE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Lifeline Systems, Inc.. It received FDA 510(k) clearance on 1991-09-27 under 510(k) number K914103. 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 LIFELINE(R) PERSONAL RESPONSE SYSTEM?

LIFELINE(R) PERSONAL RESPONSE SYSTEM is a medical device that received FDA 510(k) clearance on 1991-09-27. The listed applicant is Lifeline Systems, Inc.. The 510(k) number is K914103.

When did LIFELINE(R) PERSONAL RESPONSE SYSTEM receive FDA 510(k) clearance?

LIFELINE(R) PERSONAL RESPONSE SYSTEM received FDA 510(k) clearance on 1991-09-27, under 510(k) number K914103.

Who is the listed applicant for LIFELINE(R) PERSONAL RESPONSE SYSTEM?

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

What is the FDA product code for LIFELINE(R) PERSONAL RESPONSE SYSTEM?

The FDA product code for LIFELINE(R) PERSONAL RESPONSE SYSTEM is ILQ.

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.

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Other records listing Lifeline Systems, Inc. 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.

K103214M3810A PHILIPS TELEMONITORING SYSTEM WITH EDEVICE BRIDGED130K834441BLOOD PRESSURE MONITOR BP600XK831638SINGLE BED ARRHYTHMIA MONITOR AM500

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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