FDA 510(k)

D300 PORT ULTRASOUND LIN SCAN W/3.5 & 5.0 MHZ PROB

K-Number: K844184 · 1985-09-06

ApplicantD.R.G.

Decision Date1985-09-06

Product CodeIYO

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

D300 PORT ULTRASOUND LIN SCAN W/3.5 & 5.0 MHZ PROB is the device name listed in this FDA 510(k) record. The listed applicant is D.R.G.. It received FDA 510(k) clearance on 1985-09-06 under 510(k) number K844184. 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 D300 PORT ULTRASOUND LIN SCAN W/3.5 & 5.0 MHZ PROB?

D300 PORT ULTRASOUND LIN SCAN W/3.5 & 5.0 MHZ PROB is a medical device that received FDA 510(k) clearance on 1985-09-06. The listed applicant is D.R.G.. The 510(k) number is K844184.

When did D300 PORT ULTRASOUND LIN SCAN W/3.5 & 5.0 MHZ PROB receive FDA 510(k) clearance?

D300 PORT ULTRASOUND LIN SCAN W/3.5 & 5.0 MHZ PROB received FDA 510(k) clearance on 1985-09-06, under 510(k) number K844184.

Who is the listed applicant for D300 PORT ULTRASOUND LIN SCAN W/3.5 & 5.0 MHZ PROB?

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

What is the FDA product code for D300 PORT ULTRASOUND LIN SCAN W/3.5 & 5.0 MHZ PROB?

The FDA product code for D300 PORT ULTRASOUND LIN SCAN W/3.5 & 5.0 MHZ PROB is IYO.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.