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FDA 510(k)

ADVANTAGE

K-Number: K840120 · 1984-03-23

ApplicantGilford
Decision Date1984-03-23
Product CodeJJE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ADVANTAGE is the device name listed in this FDA 510(k) record. The listed applicant is Gilford. It received FDA 510(k) clearance on 1984-03-23 under 510(k) number K840120. The device is classified under product code JJE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADVANTAGE?

ADVANTAGE is a medical device that received FDA 510(k) clearance on 1984-03-23. The listed applicant is Gilford. The 510(k) number is K840120.

When did ADVANTAGE receive FDA 510(k) clearance?

ADVANTAGE received FDA 510(k) clearance on 1984-03-23, under 510(k) number K840120.

Who is the listed applicant for ADVANTAGE?

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

What is the FDA product code for ADVANTAGE?

The FDA product code for ADVANTAGE is JJE.

Related Clinical Trials

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.

Other records listing Gilford 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.

View all 10 devices →

Related Devices (Code: JJE)

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.

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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