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FDA 510(k)

STEAMPLUS STERILIZATION TEST

K-Number: K020409 · 2002-07-18

Decision Date2002-07-18
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STEAMPLUS STERILIZATION TEST is the device name listed in this FDA 510(k) record. The listed applicant is Spsmedical Supply Corp.. It received FDA 510(k) clearance on 2002-07-18 under 510(k) number K020409. The device is classified under product code JOJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 28 devices →

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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