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FDA 510(k)

HEMOCHRON JR. SIGNATURE +

K-Number: K020798 · 2002-03-28

ApplicantInternational Technidyne Corp.
Decision Date2002-03-28
Product CodeJPA
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

HEMOCHRON JR. SIGNATURE + 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 2002-03-28 under 510(k) number K020798. The device is classified under product code JPA. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEMOCHRON JR. SIGNATURE +?

HEMOCHRON JR. SIGNATURE + is a medical device that received FDA 510(k) clearance on 2002-03-28. The listed applicant is International Technidyne Corp.. The 510(k) number is K020798.

When did HEMOCHRON JR. SIGNATURE + receive FDA 510(k) clearance?

HEMOCHRON JR. SIGNATURE + received FDA 510(k) clearance on 2002-03-28, under 510(k) number K020798.

Who is the listed applicant for HEMOCHRON JR. SIGNATURE +?

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 HEMOCHRON JR. SIGNATURE +?

The FDA product code for HEMOCHRON JR. SIGNATURE + is JPA.

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Other records listing International Technidyne Corp. 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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