SUDORMED SWEAT PATCH SPECIMEN CONTAINER
K-Number: K902442 · 1990-10-04
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Device Summary
Frequently Asked Questions
What is the SUDORMED SWEAT PATCH SPECIMEN CONTAINER?
SUDORMED SWEAT PATCH SPECIMEN CONTAINER is a medical device that received FDA 510(k) clearance on 1990-10-04. The listed applicant is Sudormed, Inc.. The 510(k) number is K902442.
When did SUDORMED SWEAT PATCH SPECIMEN CONTAINER receive FDA 510(k) clearance?
SUDORMED SWEAT PATCH SPECIMEN CONTAINER received FDA 510(k) clearance on 1990-10-04, under 510(k) number K902442.
Who is the listed applicant for SUDORMED SWEAT PATCH SPECIMEN CONTAINER?
The FDA 510(k) record lists Sudormed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SUDORMED SWEAT PATCH SPECIMEN CONTAINER?
The FDA product code for SUDORMED SWEAT PATCH SPECIMEN CONTAINER is JKA.
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 Sudormed, 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: JKA)
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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