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FDA 510(k)

CA-1511, IN VITRO RADIOIMMUNOASSAY

K-Number: K841821 · 1984-06-22

ApplicantTravenol Laboratories, S.A.
Decision Date1984-06-22
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CA-1511, IN VITRO RADIOIMMUNOASSAY is the device name listed in this FDA 510(k) record. The listed applicant is Travenol Laboratories, S.A.. It received FDA 510(k) clearance on 1984-06-22 under 510(k) number K841821. The device is classified under product code JHI. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CA-1511, IN VITRO RADIOIMMUNOASSAY?

CA-1511, IN VITRO RADIOIMMUNOASSAY is a medical device that received FDA 510(k) clearance on 1984-06-22. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K841821.

When did CA-1511, IN VITRO RADIOIMMUNOASSAY receive FDA 510(k) clearance?

CA-1511, IN VITRO RADIOIMMUNOASSAY received FDA 510(k) clearance on 1984-06-22, under 510(k) number K841821.

Who is the listed applicant for CA-1511, IN VITRO RADIOIMMUNOASSAY?

The FDA 510(k) record lists Travenol Laboratories, S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CA-1511, IN VITRO RADIOIMMUNOASSAY?

The FDA product code for CA-1511, IN VITRO RADIOIMMUNOASSAY is JHI.

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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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