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FDA 510(k)

CATALOG NO. J-ACT+ & QC-ACT+

K-Number: K941007 · 1994-06-30

ApplicantInternational Technidyne Corp.
Decision Date1994-06-30
Product CodeJBP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

CATALOG NO. J-ACT+ & QC-ACT+ is the device name listed in this FDA 510(k) record. The listed applicant is International Technidyne Corp.. It received FDA 510(k) clearance on 1994-06-30 under 510(k) number K941007. The device is classified under product code JBP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATALOG NO. J-ACT+ & QC-ACT+?

CATALOG NO. J-ACT+ & QC-ACT+ is a medical device that received FDA 510(k) clearance on 1994-06-30. The listed applicant is International Technidyne Corp.. The 510(k) number is K941007.

When did CATALOG NO. J-ACT+ & QC-ACT+ receive FDA 510(k) clearance?

CATALOG NO. J-ACT+ & QC-ACT+ received FDA 510(k) clearance on 1994-06-30, under 510(k) number K941007.

Who is the listed applicant for CATALOG NO. J-ACT+ & QC-ACT+?

The FDA 510(k) record lists International Technidyne Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CATALOG NO. J-ACT+ & QC-ACT+?

The FDA product code for CATALOG NO. J-ACT+ & QC-ACT+ is JBP.

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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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