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FDA 510(k)

ADVANTAGE

K-Number: K921547 · 1993-07-23

ApplicantKci
Decision Date1993-07-23
Product CodeFMT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ADVANTAGE is the device name listed in this FDA 510(k) record. The listed applicant is Kci. It received FDA 510(k) clearance on 1993-07-23 under 510(k) number K921547. The device is classified under product code FMT. It was reviewed by the HO 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 1993-07-23. The listed applicant is Kci. The 510(k) number is K921547.

When did ADVANTAGE receive FDA 510(k) clearance?

ADVANTAGE received FDA 510(k) clearance on 1993-07-23, under 510(k) number K921547.

Who is the listed applicant for ADVANTAGE?

The FDA 510(k) record lists Kci 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 FMT.

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.

Related Devices (Code: FMT)

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

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