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FDA 510(k)

MEDISYS RECORD AND VERIFY SYSTEM

K-Number: K893978 · 1989-09-01

ApplicantMedisys, Inc.
Decision Date1989-09-01
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEDISYS RECORD AND VERIFY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medisys, Inc.. It received FDA 510(k) clearance on 1989-09-01 under 510(k) number K893978. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDISYS RECORD AND VERIFY SYSTEM?

MEDISYS RECORD AND VERIFY SYSTEM is a medical device that received FDA 510(k) clearance on 1989-09-01. The listed applicant is Medisys, Inc.. The 510(k) number is K893978.

When did MEDISYS RECORD AND VERIFY SYSTEM receive FDA 510(k) clearance?

MEDISYS RECORD AND VERIFY SYSTEM received FDA 510(k) clearance on 1989-09-01, under 510(k) number K893978.

Who is the listed applicant for MEDISYS RECORD AND VERIFY SYSTEM?

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

What is the FDA product code for MEDISYS RECORD AND VERIFY SYSTEM?

The FDA product code for MEDISYS RECORD AND VERIFY SYSTEM is IYE.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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