Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

BRAIN HEART INFUSION MICROBIOLOGICAL

K-Number: K801943 · 1980-09-09

Decision Date1980-09-09
Product CodeJSG
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BRAIN HEART INFUSION MICROBIOLOGICAL is the device name listed in this FDA 510(k) record. The listed applicant is Radiation Technology, Inc.. It received FDA 510(k) clearance on 1980-09-09 under 510(k) number K801943. The device is classified under product code JSG. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRAIN HEART INFUSION MICROBIOLOGICAL?

BRAIN HEART INFUSION MICROBIOLOGICAL is a medical device that received FDA 510(k) clearance on 1980-09-09. The listed applicant is Radiation Technology, Inc.. The 510(k) number is K801943.

When did BRAIN HEART INFUSION MICROBIOLOGICAL receive FDA 510(k) clearance?

BRAIN HEART INFUSION MICROBIOLOGICAL received FDA 510(k) clearance on 1980-09-09, under 510(k) number K801943.

Who is the listed applicant for BRAIN HEART INFUSION MICROBIOLOGICAL?

The FDA 510(k) record lists Radiation Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BRAIN HEART INFUSION MICROBIOLOGICAL?

The FDA product code for BRAIN HEART INFUSION MICROBIOLOGICAL is JSG.

Related Clinical Trials

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.

Other records listing Radiation Technology, Inc. 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.

View all 7 devices →

Related Devices (Code: JSG)

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.

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.

↑