FDA 510(k)

5 MHZ INTRACAVITARY PROBE, MODEL H4222V

K-Number: K860233 · 1986-06-02

Decision Date1986-06-02

Product CodeHEM

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

5 MHZ INTRACAVITARY PROBE, MODEL H4222V 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 1986-06-02 under 510(k) number K860233. The device is classified under product code HEM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 5 MHZ INTRACAVITARY PROBE, MODEL H4222V?

5 MHZ INTRACAVITARY PROBE, MODEL H4222V is a medical device that received FDA 510(k) clearance on 1986-06-02. The listed applicant is General Electric Co.. The 510(k) number is K860233.

When did 5 MHZ INTRACAVITARY PROBE, MODEL H4222V receive FDA 510(k) clearance?

5 MHZ INTRACAVITARY PROBE, MODEL H4222V received FDA 510(k) clearance on 1986-06-02, under 510(k) number K860233.

Who is the listed applicant for 5 MHZ INTRACAVITARY PROBE, MODEL H4222V?

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 5 MHZ INTRACAVITARY PROBE, MODEL H4222V?

The FDA product code for 5 MHZ INTRACAVITARY PROBE, MODEL H4222V is HEM.

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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.