BARIMEX, BARIUM SULFATE COMPOUND
K-Number: K760736 · 1976-11-09
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Device Summary
Frequently Asked Questions
What is the BARIMEX, BARIUM SULFATE COMPOUND?
BARIMEX, BARIUM SULFATE COMPOUND is a medical device that received FDA 510(k) clearance on 1976-11-09. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K760736.
When did BARIMEX, BARIUM SULFATE COMPOUND receive FDA 510(k) clearance?
BARIMEX, BARIUM SULFATE COMPOUND received FDA 510(k) clearance on 1976-11-09, under 510(k) number K760736.
Who is the listed applicant for BARIMEX, BARIUM SULFATE COMPOUND?
The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BARIMEX, BARIUM SULFATE COMPOUND?
The FDA product code for BARIMEX, BARIUM SULFATE COMPOUND is KTA.
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 C.R. Bard, 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.
Related Devices (Code: KTA)
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.
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