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FDA 510(k)

BARIUM SULFATE, USP IN SUSPENSION

K-Number: K800459 · 1980-05-30

ApplicantCentral Pharmaceuticals, Inc.
Decision Date1980-05-30
Product CodeKTA
DecisionSubstantially Equivalent

Device Summary

BARIUM SULFATE, USP IN SUSPENSION is the device name listed in this FDA 510(k) record. The listed applicant is Central Pharmaceuticals, Inc.. It received FDA 510(k) clearance on 1980-05-30 under 510(k) number K800459. The device is classified under product code KTA. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARIUM SULFATE, USP IN SUSPENSION?

BARIUM SULFATE, USP IN SUSPENSION is a medical device that received FDA 510(k) clearance on 1980-05-30. The listed applicant is Central Pharmaceuticals, Inc.. The 510(k) number is K800459.

When did BARIUM SULFATE, USP IN SUSPENSION receive FDA 510(k) clearance?

BARIUM SULFATE, USP IN SUSPENSION received FDA 510(k) clearance on 1980-05-30, under 510(k) number K800459.

Who is the listed applicant for BARIUM SULFATE, USP IN SUSPENSION?

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

What is the FDA product code for BARIUM SULFATE, USP IN SUSPENSION?

The FDA product code for BARIUM SULFATE, USP IN SUSPENSION is KTA.

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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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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