FDA 510(k)

7.5 MHZ LINEAR PROBE, CAT. NO. H4221H

K-Number: K862844 · 1986-11-25

Decision Date1986-11-25

Product CodeITX

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

7.5 MHZ LINEAR PROBE, CAT. NO. H4221H 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 1986-11-25 under 510(k) number K862844. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 7.5 MHZ LINEAR PROBE, CAT. NO. H4221H?

7.5 MHZ LINEAR PROBE, CAT. NO. H4221H is a medical device that received FDA 510(k) clearance on 1986-11-25. The listed applicant is General Electric Co.. The 510(k) number is K862844.

When did 7.5 MHZ LINEAR PROBE, CAT. NO. H4221H receive FDA 510(k) clearance?

7.5 MHZ LINEAR PROBE, CAT. NO. H4221H received FDA 510(k) clearance on 1986-11-25, under 510(k) number K862844.

Who is the listed applicant for 7.5 MHZ LINEAR PROBE, CAT. NO. H4221H?

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 7.5 MHZ LINEAR PROBE, CAT. NO. H4221H?

The FDA product code for 7.5 MHZ LINEAR PROBE, CAT. NO. H4221H is ITX.

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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.