PAB IV CONTAINER
K-Number: K840388 · 1984-03-06
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Device Summary
Frequently Asked Questions
What is the PAB IV CONTAINER?
PAB IV CONTAINER is a medical device that received FDA 510(k) clearance on 1984-03-06. The listed applicant is American Mcgaw. The 510(k) number is K840388.
When did PAB IV CONTAINER receive FDA 510(k) clearance?
PAB IV CONTAINER received FDA 510(k) clearance on 1984-03-06, under 510(k) number K840388.
Who is the listed applicant for PAB IV CONTAINER?
The FDA 510(k) record lists American Mcgaw as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PAB IV CONTAINER?
The FDA product code for PAB IV CONTAINER is KPE.
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 American Mcgaw 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: KPE)
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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