FDA 510(k)

MECHANICAL SECTOR PROBE 4 MHZ DFM

K-Number: K842880 · 1984-12-10

Decision Date1984-12-10

Product CodeIYO

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

MECHANICAL SECTOR PROBE 4 MHZ DFM is the device name listed in this FDA 510(k) record. The listed applicant is General Electric Co.. It received FDA 510(k) clearance on 1984-12-10 under 510(k) number K842880. 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 MECHANICAL SECTOR PROBE 4 MHZ DFM?

MECHANICAL SECTOR PROBE 4 MHZ DFM is a medical device that received FDA 510(k) clearance on 1984-12-10. The listed applicant is General Electric Co.. The 510(k) number is K842880.

When did MECHANICAL SECTOR PROBE 4 MHZ DFM receive FDA 510(k) clearance?

MECHANICAL SECTOR PROBE 4 MHZ DFM received FDA 510(k) clearance on 1984-12-10, under 510(k) number K842880.

Who is the listed applicant for MECHANICAL SECTOR PROBE 4 MHZ DFM?

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

What is the FDA product code for MECHANICAL SECTOR PROBE 4 MHZ DFM?

The FDA product code for MECHANICAL SECTOR PROBE 4 MHZ DFM 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.