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FDA 510(k)

7620 REMOTE CENTRAL STATION REPEATER

K-Number: K901884 · 1990-06-12

Decision Date1990-06-12
Product CodeDXJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

7620 REMOTE CENTRAL STATION REPEATER 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 1990-06-12 under 510(k) number K901884. The device is classified under product code DXJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 7620 REMOTE CENTRAL STATION REPEATER?

7620 REMOTE CENTRAL STATION REPEATER is a medical device that received FDA 510(k) clearance on 1990-06-12. The listed applicant is Marquette Electronics, Inc.. The 510(k) number is K901884.

When did 7620 REMOTE CENTRAL STATION REPEATER receive FDA 510(k) clearance?

7620 REMOTE CENTRAL STATION REPEATER received FDA 510(k) clearance on 1990-06-12, under 510(k) number K901884.

Who is the listed applicant for 7620 REMOTE CENTRAL STATION REPEATER?

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 7620 REMOTE CENTRAL STATION REPEATER?

The FDA product code for 7620 REMOTE CENTRAL STATION REPEATER is DXJ.

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.

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.

View all 82 devices →

Related Devices (Code: DXJ)

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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