FDA 510(k)

AUTOFOCUS DUAL ELEMENT PROBE

K-Number: K842777 · 1984-11-29

Decision Date1984-11-29

Product CodeIYO

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

AUTOFOCUS DUAL ELEMENT PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Technicare Corp.. It received FDA 510(k) clearance on 1984-11-29 under 510(k) number K842777. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOFOCUS DUAL ELEMENT PROBE?

AUTOFOCUS DUAL ELEMENT PROBE is a medical device that received FDA 510(k) clearance on 1984-11-29. The listed applicant is Technicare Corp.. The 510(k) number is K842777.

When did AUTOFOCUS DUAL ELEMENT PROBE receive FDA 510(k) clearance?

AUTOFOCUS DUAL ELEMENT PROBE received FDA 510(k) clearance on 1984-11-29, under 510(k) number K842777.

Who is the listed applicant for AUTOFOCUS DUAL ELEMENT PROBE?

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 AUTOFOCUS DUAL ELEMENT PROBE?

The FDA product code for AUTOFOCUS DUAL ELEMENT PROBE is IYO.

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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.