FDA 510(k)

DELUXE ADJUSTABLE HEIGHT ULTRASOUND TABLE

K-Number: K922604 · 1992-10-20

Decision Date1992-10-20

Product CodeIYO

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

DELUXE ADJUSTABLE HEIGHT ULTRASOUND TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Biodan Medical Systems, Ltd.. It received FDA 510(k) clearance on 1992-10-20 under 510(k) number K922604. 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 DELUXE ADJUSTABLE HEIGHT ULTRASOUND TABLE?

DELUXE ADJUSTABLE HEIGHT ULTRASOUND TABLE is a medical device that received FDA 510(k) clearance on 1992-10-20. The listed applicant is Biodan Medical Systems, Ltd.. The 510(k) number is K922604.

When did DELUXE ADJUSTABLE HEIGHT ULTRASOUND TABLE receive FDA 510(k) clearance?

DELUXE ADJUSTABLE HEIGHT ULTRASOUND TABLE received FDA 510(k) clearance on 1992-10-20, under 510(k) number K922604.

Who is the listed applicant for DELUXE ADJUSTABLE HEIGHT ULTRASOUND TABLE?

The FDA 510(k) record lists Biodan Medical Systems, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DELUXE ADJUSTABLE HEIGHT ULTRASOUND TABLE?

The FDA product code for DELUXE ADJUSTABLE HEIGHT ULTRASOUND TABLE 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.