FDA 510(k)

CVA

K-Number: K833967 · 1984-01-11

Decision Date1984-01-11

Product CodeJSJ

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

CVA is the device name listed in this FDA 510(k) record. The listed applicant is Remel Co.. It received FDA 510(k) clearance on 1984-01-11 under 510(k) number K833967. The device is classified under product code JSJ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CVA?

CVA is a medical device that received FDA 510(k) clearance on 1984-01-11. The listed applicant is Remel Co.. The 510(k) number is K833967.

When did CVA receive FDA 510(k) clearance?

CVA received FDA 510(k) clearance on 1984-01-11, under 510(k) number K833967.

Who is the listed applicant for CVA?

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

What is the FDA product code for CVA?

The FDA product code for CVA is JSJ.

Other records listing Remel Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K013711BACTI-SWAB DRY K965151A.C.T. III K965150A.C.T. IV K965152A.C.T. II K965149A.C.T. I K960090CALCOFLUOR WHITE STAIN KIT

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Related Devices (Code: JSJ)

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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.