STERILIZATION CONTAINER
K-Number: K833343 · 1983-11-03
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Device Summary
Frequently Asked Questions
What is the STERILIZATION CONTAINER?
STERILIZATION CONTAINER is a medical device that received FDA 510(k) clearance on 1983-11-03. The listed applicant is Medin Corp.. The 510(k) number is K833343.
When did STERILIZATION CONTAINER receive FDA 510(k) clearance?
STERILIZATION CONTAINER received FDA 510(k) clearance on 1983-11-03, under 510(k) number K833343.
Who is the listed applicant for STERILIZATION CONTAINER?
The FDA 510(k) record lists Medin Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STERILIZATION CONTAINER?
The FDA product code for STERILIZATION CONTAINER is FRG.
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 Medin Corp. 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: FRG)
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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