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FDA 510(k)

ULTRASYSTEM LINSCAN PROBE

K-Number: K842811 · 1984-09-17

ApplicantKelley Development Corp.
Decision Date1984-09-17
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ULTRASYSTEM LINSCAN PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Kelley Development Corp.. It received FDA 510(k) clearance on 1984-09-17 under 510(k) number K842811. 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 ULTRASYSTEM LINSCAN PROBE?

ULTRASYSTEM LINSCAN PROBE is a medical device that received FDA 510(k) clearance on 1984-09-17. The listed applicant is Kelley Development Corp.. The 510(k) number is K842811.

When did ULTRASYSTEM LINSCAN PROBE receive FDA 510(k) clearance?

ULTRASYSTEM LINSCAN PROBE received FDA 510(k) clearance on 1984-09-17, under 510(k) number K842811.

Who is the listed applicant for ULTRASYSTEM LINSCAN PROBE?

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

What is the FDA product code for ULTRASYSTEM LINSCAN PROBE?

The FDA product code for ULTRASYSTEM LINSCAN 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.

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