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FDA 510(k)

CT PACE CATALOG NUMBER B7950A

K-Number: K872526 · 1987-09-23

ApplicantGeneral Electric Co.
Decision Date1987-09-23
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CT PACE CATALOG NUMBER B7950A 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 1987-09-23 under 510(k) number K872526. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CT PACE CATALOG NUMBER B7950A?

CT PACE CATALOG NUMBER B7950A is a medical device that received FDA 510(k) clearance on 1987-09-23. The listed applicant is General Electric Co.. The 510(k) number is K872526.

When did CT PACE CATALOG NUMBER B7950A receive FDA 510(k) clearance?

CT PACE CATALOG NUMBER B7950A received FDA 510(k) clearance on 1987-09-23, under 510(k) number K872526.

Who is the listed applicant for CT PACE CATALOG NUMBER B7950A?

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 CT PACE CATALOG NUMBER B7950A?

The FDA product code for CT PACE CATALOG NUMBER B7950A is JAK.

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Related Devices (Code: JAK)

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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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