DUSTCOVERS/STERILITY MAINTENANCE COVERS
K-Number: K831165 · 1983-05-03
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Device Summary
Frequently Asked Questions
What is the DUSTCOVERS/STERILITY MAINTENANCE COVERS?
DUSTCOVERS/STERILITY MAINTENANCE COVERS is a medical device that received FDA 510(k) clearance on 1983-05-03. The listed applicant is Medical Industries Packaging, Inc.. The 510(k) number is K831165.
When did DUSTCOVERS/STERILITY MAINTENANCE COVERS receive FDA 510(k) clearance?
DUSTCOVERS/STERILITY MAINTENANCE COVERS received FDA 510(k) clearance on 1983-05-03, under 510(k) number K831165.
Who is the listed applicant for DUSTCOVERS/STERILITY MAINTENANCE COVERS?
The FDA 510(k) record lists Medical Industries Packaging, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DUSTCOVERS/STERILITY MAINTENANCE COVERS?
The FDA product code for DUSTCOVERS/STERILITY MAINTENANCE COVERS 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 Medical Industries Packaging, 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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