FDA 510(k)

CHRONOCOR VI MODEL 5012

K-Number: K915364 · 1992-02-07

Decision Date1992-02-07

Product CodeDTE

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CHRONOCOR VI MODEL 5012 is the device name listed in this FDA 510(k) record. The listed applicant is Seamed Corp.. It received FDA 510(k) clearance on 1992-02-07 under 510(k) number K915364. The device is classified under product code DTE. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHRONOCOR VI MODEL 5012?

CHRONOCOR VI MODEL 5012 is a medical device that received FDA 510(k) clearance on 1992-02-07. The listed applicant is Seamed Corp.. The 510(k) number is K915364.

When did CHRONOCOR VI MODEL 5012 receive FDA 510(k) clearance?

CHRONOCOR VI MODEL 5012 received FDA 510(k) clearance on 1992-02-07, under 510(k) number K915364.

Who is the listed applicant for CHRONOCOR VI MODEL 5012?

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

What is the FDA product code for CHRONOCOR VI MODEL 5012?

The FDA product code for CHRONOCOR VI MODEL 5012 is DTE.

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Other records listing Seamed Corp. as applicant

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Related Devices (Code: DTE)

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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.