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FDA 510(k)

MEDCUFF

K-Number: K942488 · 1994-08-23

ApplicantMed-Con, Inc.
Decision Date1994-08-23
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDCUFF is the device name listed in this FDA 510(k) record. The listed applicant is Med-Con, Inc.. It received FDA 510(k) clearance on 1994-08-23 under 510(k) number K942488. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDCUFF?

MEDCUFF is a medical device that received FDA 510(k) clearance on 1994-08-23. The listed applicant is Med-Con, Inc.. The 510(k) number is K942488.

When did MEDCUFF receive FDA 510(k) clearance?

MEDCUFF received FDA 510(k) clearance on 1994-08-23, under 510(k) number K942488.

Who is the listed applicant for MEDCUFF?

The FDA 510(k) record lists Med-Con, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDCUFF?

The FDA product code for MEDCUFF is DXQ.

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 Med-Con, 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.

Related Devices (Code: DXQ)

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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