MILTEX RIGID CONTAINER SYSTEMS
K-Number: K072563 · 2008-02-12
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Device Summary
Frequently Asked Questions
What is the MILTEX RIGID CONTAINER SYSTEMS?
MILTEX RIGID CONTAINER SYSTEMS is a medical device that received FDA 510(k) clearance on 2008-02-12. The listed applicant is Miltex, Inc.. The 510(k) number is K072563.
When did MILTEX RIGID CONTAINER SYSTEMS receive FDA 510(k) clearance?
MILTEX RIGID CONTAINER SYSTEMS received FDA 510(k) clearance on 2008-02-12, under 510(k) number K072563.
Who is the listed applicant for MILTEX RIGID CONTAINER SYSTEMS?
The FDA 510(k) record lists Miltex, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MILTEX RIGID CONTAINER SYSTEMS?
The FDA product code for MILTEX RIGID CONTAINER SYSTEMS is KCT.
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 Miltex, 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: KCT)
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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