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FDA 510(k)

BI-4520 DUAL IMPEDOMETER

K-Number: K821723 · 1982-09-15

ApplicantFarrall Instruments, Inc.
Decision Date1982-09-15
Product Code
DecisionSubstantially Equivalent

Device Summary

BI-4520 DUAL IMPEDOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Farrall Instruments, Inc.. It received FDA 510(k) clearance on 1982-09-15 under 510(k) number K821723. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BI-4520 DUAL IMPEDOMETER?

BI-4520 DUAL IMPEDOMETER is a medical device that received FDA 510(k) clearance on 1982-09-15. The listed applicant is Farrall Instruments, Inc.. The 510(k) number is K821723.

When did BI-4520 DUAL IMPEDOMETER receive FDA 510(k) clearance?

BI-4520 DUAL IMPEDOMETER received FDA 510(k) clearance on 1982-09-15, under 510(k) number K821723.

Who is the listed applicant for BI-4520 DUAL IMPEDOMETER?

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

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Other records listing Farrall Instruments, Inc. as applicant

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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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