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FDA 510(k)

I BRADYKININ & ANTI-BRADYKININ ANTISERUM

K-Number: K790362 · 1979-04-23

ApplicantCambridge Nuclear Corp.
Decision Date1979-04-23
Product Code
DecisionSubstantially Equivalent

Device Summary

I BRADYKININ & ANTI-BRADYKININ ANTISERUM is the device name listed in this FDA 510(k) record. The listed applicant is Cambridge Nuclear Corp.. It received FDA 510(k) clearance on 1979-04-23 under 510(k) number K790362. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the I BRADYKININ & ANTI-BRADYKININ ANTISERUM?

I BRADYKININ & ANTI-BRADYKININ ANTISERUM is a medical device that received FDA 510(k) clearance on 1979-04-23. The listed applicant is Cambridge Nuclear Corp.. The 510(k) number is K790362.

When did I BRADYKININ & ANTI-BRADYKININ ANTISERUM receive FDA 510(k) clearance?

I BRADYKININ & ANTI-BRADYKININ ANTISERUM received FDA 510(k) clearance on 1979-04-23, under 510(k) number K790362.

Who is the listed applicant for I BRADYKININ & ANTI-BRADYKININ ANTISERUM?

The FDA 510(k) record lists Cambridge Nuclear Corp. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Cambridge Nuclear Corp. as applicant

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.

K811380ESTRIOL KITK810804PROGESTERONE KITK790007I TESTOTERONEK790008I ESTRIOL

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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