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FDA 510(k)

STERITEC DISPOSABLE INTEGRATOR LOAD CHALLENGE-STEAM

K-Number: K965212 · 1998-04-23

Decision Date1998-04-23
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERITEC DISPOSABLE INTEGRATOR LOAD CHALLENGE-STEAM is the device name listed in this FDA 510(k) record. The listed applicant is Steritec Products Mfg Co, Inc.. It received FDA 510(k) clearance on 1998-04-23 under 510(k) number K965212. 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 STERITEC DISPOSABLE INTEGRATOR LOAD CHALLENGE-STEAM?

STERITEC DISPOSABLE INTEGRATOR LOAD CHALLENGE-STEAM is a medical device that received FDA 510(k) clearance on 1998-04-23. The listed applicant is Steritec Products Mfg Co, Inc.. The 510(k) number is K965212.

When did STERITEC DISPOSABLE INTEGRATOR LOAD CHALLENGE-STEAM receive FDA 510(k) clearance?

STERITEC DISPOSABLE INTEGRATOR LOAD CHALLENGE-STEAM received FDA 510(k) clearance on 1998-04-23, under 510(k) number K965212.

Who is the listed applicant for STERITEC DISPOSABLE INTEGRATOR LOAD CHALLENGE-STEAM?

The FDA 510(k) record lists Steritec Products Mfg Co, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERITEC DISPOSABLE INTEGRATOR LOAD CHALLENGE-STEAM?

The FDA product code for STERITEC DISPOSABLE INTEGRATOR LOAD CHALLENGE-STEAM 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 Steritec Products Mfg Co, 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.

View all 20 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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