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FDA 510(k)

RF TEST KIT

K-Number: K841454 · 1984-04-25

ApplicantDifco Laboratories, Inc.
Decision Date1984-04-25
Product CodeDHR
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

RF TEST KIT is the device name listed in this FDA 510(k) record. The listed applicant is Difco Laboratories, Inc.. It received FDA 510(k) clearance on 1984-04-25 under 510(k) number K841454. The device is classified under product code DHR. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RF TEST KIT?

RF TEST KIT is a medical device that received FDA 510(k) clearance on 1984-04-25. The listed applicant is Difco Laboratories, Inc.. The 510(k) number is K841454.

When did RF TEST KIT receive FDA 510(k) clearance?

RF TEST KIT received FDA 510(k) clearance on 1984-04-25, under 510(k) number K841454.

Who is the listed applicant for RF TEST KIT?

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

What is the FDA product code for RF TEST KIT?

The FDA product code for RF TEST KIT is DHR.

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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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