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FDA 510(k)

SERIES 1500 RESPONDER

K-Number: K902782 · 1991-01-18

ApplicantMarquette Electronics, Inc.
Decision Date1991-01-18
Product CodeLDD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SERIES 1500 RESPONDER is the device name listed in this FDA 510(k) record. The listed applicant is Marquette Electronics, Inc.. It received FDA 510(k) clearance on 1991-01-18 under 510(k) number K902782. The device is classified under product code LDD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERIES 1500 RESPONDER?

SERIES 1500 RESPONDER is a medical device that received FDA 510(k) clearance on 1991-01-18. The listed applicant is Marquette Electronics, Inc.. The 510(k) number is K902782.

When did SERIES 1500 RESPONDER receive FDA 510(k) clearance?

SERIES 1500 RESPONDER received FDA 510(k) clearance on 1991-01-18, under 510(k) number K902782.

Who is the listed applicant for SERIES 1500 RESPONDER?

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

What is the FDA product code for SERIES 1500 RESPONDER?

The FDA product code for SERIES 1500 RESPONDER is LDD.

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Other records listing Marquette Electronics, 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.

K971868IMPACT (INFORMING MOBILE PERSONNEL AND CARE TRACKING) PAGER SYSTEMK971683WIRELESS LAN (LOCAL AREA NETWORK) - WIRELESS ETHERNETK972199SIGNAL-AVERAGED HIGH RESOLUTION P WAVE ANALYSISK962547CARDIOSERV PK963120RESPONDER 2500 DEFIBRILLATOR AND CARDIAC CARE SYSTEMK962827ALARM DISPLAY UNIT/PAGER-LAN SYSTEM (ADU)

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Related Devices (Code: LDD)

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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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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