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FDA 510(k)

RENNER-PLAN

K-Number: K894722 · 1990-01-03

ApplicantW.D. Renner Consulting Co.
Decision Date1990-01-03
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RENNER-PLAN is the device name listed in this FDA 510(k) record. The listed applicant is W.D. Renner Consulting Co.. It received FDA 510(k) clearance on 1990-01-03 under 510(k) number K894722. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RENNER-PLAN?

RENNER-PLAN is a medical device that received FDA 510(k) clearance on 1990-01-03. The listed applicant is W.D. Renner Consulting Co.. The 510(k) number is K894722.

When did RENNER-PLAN receive FDA 510(k) clearance?

RENNER-PLAN received FDA 510(k) clearance on 1990-01-03, under 510(k) number K894722.

Who is the listed applicant for RENNER-PLAN?

The FDA 510(k) record lists W.D. Renner Consulting Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RENNER-PLAN?

The FDA product code for RENNER-PLAN is IYE.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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