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FDA 510(k)

STERITEC INTEGRAPH MODEL CI-101

K-Number: K960441 · 1997-05-08

ApplicantSteritec Products Mfg Co, Inc.
Decision Date1997-05-08
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERITEC INTEGRAPH MODEL CI-101 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 1997-05-08 under 510(k) number K960441. 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 INTEGRAPH MODEL CI-101?

STERITEC INTEGRAPH MODEL CI-101 is a medical device that received FDA 510(k) clearance on 1997-05-08. The listed applicant is Steritec Products Mfg Co, Inc.. The 510(k) number is K960441.

When did STERITEC INTEGRAPH MODEL CI-101 receive FDA 510(k) clearance?

STERITEC INTEGRAPH MODEL CI-101 received FDA 510(k) clearance on 1997-05-08, under 510(k) number K960441.

Who is the listed applicant for STERITEC INTEGRAPH MODEL CI-101?

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 INTEGRAPH MODEL CI-101?

The FDA product code for STERITEC INTEGRAPH MODEL CI-101 is JOJ.

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Other records listing Steritec Products Mfg Co, Inc. as applicant

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Related Devices (Code: JOJ)

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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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