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FDA 510(k)

IMPEDANCE TESTER (MODEL 4390)

K-Number: K760776 · 1976-10-08

ApplicantCambridge Instruments, Inc.
Decision Date1976-10-08
Product Code
DecisionSubstantially Equivalent

Device Summary

IMPEDANCE TESTER (MODEL 4390) is the device name listed in this FDA 510(k) record. The listed applicant is Cambridge Instruments, Inc.. It received FDA 510(k) clearance on 1976-10-08 under 510(k) number K760776. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPEDANCE TESTER (MODEL 4390)?

IMPEDANCE TESTER (MODEL 4390) is a medical device that received FDA 510(k) clearance on 1976-10-08. The listed applicant is Cambridge Instruments, Inc.. The 510(k) number is K760776.

When did IMPEDANCE TESTER (MODEL 4390) receive FDA 510(k) clearance?

IMPEDANCE TESTER (MODEL 4390) received FDA 510(k) clearance on 1976-10-08, under 510(k) number K760776.

Who is the listed applicant for IMPEDANCE TESTER (MODEL 4390)?

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

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Other records listing Cambridge Instruments, 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.

K811121CENTRAL STATION MONITORING SYSTEMSK811062CAMPBRIDGE COMPUTRACEK8032294-CHANNEL ECG TELEMETRY MON. SYST. #3045K801224CAMBRIDGE CARDIAC DIAGNOSTIC SYSTEMK800566CAMBRIDGE VS-550 ELECTROCARDIOGRAPHK792661TREADMILL MODEL 3060

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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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