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FDA 510(k)

INTEGRAPH FLASH, MODEL CI 110

K-Number: K012732 · 2002-03-04

ApplicantSteritec Products, Inc.
Decision Date2002-03-04
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INTEGRAPH FLASH, MODEL CI 110 is the device name listed in this FDA 510(k) record. The listed applicant is Steritec Products, Inc.. It received FDA 510(k) clearance on 2002-03-04 under 510(k) number K012732. 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 INTEGRAPH FLASH, MODEL CI 110?

INTEGRAPH FLASH, MODEL CI 110 is a medical device that received FDA 510(k) clearance on 2002-03-04. The listed applicant is Steritec Products, Inc.. The 510(k) number is K012732.

When did INTEGRAPH FLASH, MODEL CI 110 receive FDA 510(k) clearance?

INTEGRAPH FLASH, MODEL CI 110 received FDA 510(k) clearance on 2002-03-04, under 510(k) number K012732.

Who is the listed applicant for INTEGRAPH FLASH, MODEL CI 110?

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

What is the FDA product code for INTEGRAPH FLASH, MODEL CI 110?

The FDA product code for INTEGRAPH FLASH, MODEL CI 110 is JOJ.

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Other records listing Steritec Products, Inc. as applicant

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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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