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FDA 510(k)

CMS RECORD AND VERIFY SYSTEM

K-Number: K882484 · 1988-12-21

ApplicantComputerized Medical Systems, Inc.
Decision Date1988-12-21
Product CodeJAD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CMS RECORD AND VERIFY SYSTEM 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 1988-12-21 under 510(k) number K882484. The device is classified under product code JAD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CMS RECORD AND VERIFY SYSTEM?

CMS RECORD AND VERIFY SYSTEM is a medical device that received FDA 510(k) clearance on 1988-12-21. The listed applicant is Computerized Medical Systems, Inc.. The 510(k) number is K882484.

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

CMS RECORD AND VERIFY SYSTEM received FDA 510(k) clearance on 1988-12-21, under 510(k) number K882484.

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

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 CMS RECORD AND VERIFY SYSTEM?

The FDA product code for CMS RECORD AND VERIFY SYSTEM is JAD.

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Other records listing Computerized Medical Systems, Inc. as applicant

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Related Devices (Code: JAD)

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.

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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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