STEAMPLUS STERILIZATION TEST
K-Number: K020409 · 2002-07-18
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Device Summary
Frequently Asked Questions
What is the STEAMPLUS STERILIZATION TEST?
STEAMPLUS STERILIZATION TEST is a medical device that received FDA 510(k) clearance on 2002-07-18. The listed applicant is Spsmedical Supply Corp.. The 510(k) number is K020409.
When did STEAMPLUS STERILIZATION TEST receive FDA 510(k) clearance?
STEAMPLUS STERILIZATION TEST received FDA 510(k) clearance on 2002-07-18, under 510(k) number K020409.
Who is the listed applicant for STEAMPLUS STERILIZATION TEST?
The FDA 510(k) record lists Spsmedical Supply Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STEAMPLUS STERILIZATION TEST?
The FDA product code for STEAMPLUS STERILIZATION TEST is JOJ.
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 Spsmedical Supply 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: JOJ)
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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