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FDA 510(k)

AUTO-CUFF(TM)

K-Number: K896633 · 1990-02-01

ApplicantU.S. Medical Corp.
Decision Date1990-02-01
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AUTO-CUFF(TM) is the device name listed in this FDA 510(k) record. The listed applicant is U.S. Medical Corp.. It received FDA 510(k) clearance on 1990-02-01 under 510(k) number K896633. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTO-CUFF(TM)?

AUTO-CUFF(TM) is a medical device that received FDA 510(k) clearance on 1990-02-01. The listed applicant is U.S. Medical Corp.. The 510(k) number is K896633.

When did AUTO-CUFF(TM) receive FDA 510(k) clearance?

AUTO-CUFF(TM) received FDA 510(k) clearance on 1990-02-01, under 510(k) number K896633.

Who is the listed applicant for AUTO-CUFF(TM)?

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

What is the FDA product code for AUTO-CUFF(TM)?

The FDA product code for AUTO-CUFF(TM) is DXN.

Other records listing U.S. Medical Corp. 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: DXN)

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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