DUSTCOVERS &/OR STERILITY MAINT. COVERS
K-Number: K821332 · 1982-05-27
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Device Summary
Frequently Asked Questions
What is the DUSTCOVERS &/OR STERILITY MAINT. COVERS?
DUSTCOVERS &/OR STERILITY MAINT. COVERS is a medical device that received FDA 510(k) clearance on 1982-05-27. The listed applicant is Medical Industries Packaging, Inc.. The 510(k) number is K821332.
When did DUSTCOVERS &/OR STERILITY MAINT. COVERS receive FDA 510(k) clearance?
DUSTCOVERS &/OR STERILITY MAINT. COVERS received FDA 510(k) clearance on 1982-05-27, under 510(k) number K821332.
Who is the listed applicant for DUSTCOVERS &/OR STERILITY MAINT. 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 &/OR STERILITY MAINT. COVERS?
The FDA product code for DUSTCOVERS &/OR STERILITY MAINT. 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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