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FDA 510(k)

RECORD AND VERIFY MEVATRON ADAPTER

K-Number: K913674 · 1991-11-22

ApplicantComputerized Medical Systems, Inc.
Decision Date1991-11-22
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RECORD AND VERIFY MEVATRON ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is Computerized Medical Systems, Inc.. It received FDA 510(k) clearance on 1991-11-22 under 510(k) number K913674. 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 RECORD AND VERIFY MEVATRON ADAPTER?

RECORD AND VERIFY MEVATRON ADAPTER is a medical device that received FDA 510(k) clearance on 1991-11-22. The listed applicant is Computerized Medical Systems, Inc.. The 510(k) number is K913674.

When did RECORD AND VERIFY MEVATRON ADAPTER receive FDA 510(k) clearance?

RECORD AND VERIFY MEVATRON ADAPTER received FDA 510(k) clearance on 1991-11-22, under 510(k) number K913674.

Who is the listed applicant for RECORD AND VERIFY MEVATRON ADAPTER?

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

What is the FDA product code for RECORD AND VERIFY MEVATRON ADAPTER?

The FDA product code for RECORD AND VERIFY MEVATRON ADAPTER is IYE.

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Other records listing Computerized Medical Systems, Inc. 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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