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FDA 510(k)

REAGENT SET, RENORPACE

K-Number: K770765 · 1977-06-24

ApplicantG.D. Searle and Co.
Decision Date1977-06-24
Product CodeDPA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

REAGENT SET, RENORPACE 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 1977-06-24 under 510(k) number K770765. The device is classified under product code DPA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REAGENT SET, RENORPACE?

REAGENT SET, RENORPACE is a medical device that received FDA 510(k) clearance on 1977-06-24. The listed applicant is G.D. Searle and Co.. The 510(k) number is K770765.

When did REAGENT SET, RENORPACE receive FDA 510(k) clearance?

REAGENT SET, RENORPACE received FDA 510(k) clearance on 1977-06-24, under 510(k) number K770765.

Who is the listed applicant for REAGENT SET, RENORPACE?

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 REAGENT SET, RENORPACE?

The FDA product code for REAGENT SET, RENORPACE is DPA.

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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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