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FDA 510(k)

CENTRAL DISPLAY SYSTEM #CS400

K-Number: K821479 · 1982-06-25

ApplicantAdvantage Medical Systems, Inc.
Decision Date1982-06-25
Product CodeHGM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CENTRAL DISPLAY SYSTEM #CS400 is the device name listed in this FDA 510(k) record. The listed applicant is Advantage Medical Systems, Inc.. It received FDA 510(k) clearance on 1982-06-25 under 510(k) number K821479. The device is classified under product code HGM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTRAL DISPLAY SYSTEM #CS400?

CENTRAL DISPLAY SYSTEM #CS400 is a medical device that received FDA 510(k) clearance on 1982-06-25. The listed applicant is Advantage Medical Systems, Inc.. The 510(k) number is K821479.

When did CENTRAL DISPLAY SYSTEM #CS400 receive FDA 510(k) clearance?

CENTRAL DISPLAY SYSTEM #CS400 received FDA 510(k) clearance on 1982-06-25, under 510(k) number K821479.

Who is the listed applicant for CENTRAL DISPLAY SYSTEM #CS400?

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

What is the FDA product code for CENTRAL DISPLAY SYSTEM #CS400?

The FDA product code for CENTRAL DISPLAY SYSTEM #CS400 is HGM.

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Other records listing Advantage Medical Systems, Inc. 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.

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Related Devices (Code: HGM)

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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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