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FDA 510(k)

RIA CONTROLS

K-Number: K781593 · 1978-10-17

ApplicantDade, Baxter Travenol Diagnostics, Inc.
Decision Date1978-10-17
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

RIA CONTROLS is the device name listed in this FDA 510(k) record. The listed applicant is Dade, Baxter Travenol Diagnostics, Inc.. It received FDA 510(k) clearance on 1978-10-17 under 510(k) number K781593. The device is classified under product code JJY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIA CONTROLS?

RIA CONTROLS is a medical device that received FDA 510(k) clearance on 1978-10-17. The listed applicant is Dade, Baxter Travenol Diagnostics, Inc.. The 510(k) number is K781593.

When did RIA CONTROLS receive FDA 510(k) clearance?

RIA CONTROLS received FDA 510(k) clearance on 1978-10-17, under 510(k) number K781593.

Who is the listed applicant for RIA CONTROLS?

The FDA 510(k) record lists Dade, Baxter Travenol Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RIA CONTROLS?

The FDA product code for RIA CONTROLS is JJY.

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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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