FDA 510(k)

AUTO DII MULTI FREQUENCY

K-Number: K844293 · 1985-02-13

Decision Date1985-02-13

Product CodeIYN

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

AUTO DII MULTI FREQUENCY is the device name listed in this FDA 510(k) record. The listed applicant is Technicare Corp.. It received FDA 510(k) clearance on 1985-02-13 under 510(k) number K844293. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTO DII MULTI FREQUENCY?

AUTO DII MULTI FREQUENCY is a medical device that received FDA 510(k) clearance on 1985-02-13. The listed applicant is Technicare Corp.. The 510(k) number is K844293.

When did AUTO DII MULTI FREQUENCY receive FDA 510(k) clearance?

AUTO DII MULTI FREQUENCY received FDA 510(k) clearance on 1985-02-13, under 510(k) number K844293.

Who is the listed applicant for AUTO DII MULTI FREQUENCY?

The FDA 510(k) record lists Technicare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUTO DII MULTI FREQUENCY?

The FDA product code for AUTO DII MULTI FREQUENCY is IYN.

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Other records listing Technicare Corp. 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.