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FDA 510(k)

VTX (GE CATAOLG NO. B7005A)

K-Number: K792067 · 1979-12-10

ApplicantGeneral Electric Co.
Decision Date1979-12-10
Product CodeIZF
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VTX (GE CATAOLG NO. B7005A) 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 1979-12-10 under 510(k) number K792067. The device is classified under product code IZF. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VTX (GE CATAOLG NO. B7005A)?

VTX (GE CATAOLG NO. B7005A) is a medical device that received FDA 510(k) clearance on 1979-12-10. The listed applicant is General Electric Co.. The 510(k) number is K792067.

When did VTX (GE CATAOLG NO. B7005A) receive FDA 510(k) clearance?

VTX (GE CATAOLG NO. B7005A) received FDA 510(k) clearance on 1979-12-10, under 510(k) number K792067.

Who is the listed applicant for VTX (GE CATAOLG NO. B7005A)?

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 VTX (GE CATAOLG NO. B7005A)?

The FDA product code for VTX (GE CATAOLG NO. B7005A) is IZF.

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Other records listing General Electric Co. as applicant

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Related Devices (Code: IZF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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