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FDA 510(k)

RADIOASSAY TUBES & RADIOASSAY TUBE CAPS

K-Number: K770740 · 1977-06-22

ApplicantG.D. Searle and Co.
Decision Date1977-06-22
Product CodeJJJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

RADIOASSAY TUBES & RADIOASSAY TUBE CAPS is the device name listed in this FDA 510(k) record. The listed applicant is G.D. Searle and Co.. It received FDA 510(k) clearance on 1977-06-22 under 510(k) number K770740. The device is classified under product code JJJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADIOASSAY TUBES & RADIOASSAY TUBE CAPS?

RADIOASSAY TUBES & RADIOASSAY TUBE CAPS is a medical device that received FDA 510(k) clearance on 1977-06-22. The listed applicant is G.D. Searle and Co.. The 510(k) number is K770740.

When did RADIOASSAY TUBES & RADIOASSAY TUBE CAPS receive FDA 510(k) clearance?

RADIOASSAY TUBES & RADIOASSAY TUBE CAPS received FDA 510(k) clearance on 1977-06-22, under 510(k) number K770740.

Who is the listed applicant for RADIOASSAY TUBES & RADIOASSAY TUBE CAPS?

The FDA 510(k) record lists G.D. Searle and Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RADIOASSAY TUBES & RADIOASSAY TUBE CAPS?

The FDA product code for RADIOASSAY TUBES & RADIOASSAY TUBE CAPS is JJJ.

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Other records listing G.D. Searle and Co. as applicant

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Related Devices (Code: JJJ)

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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