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FDA 510(k)

CLEAN CUFF BLOOD PRESSURE CUFF LINER

K-Number: K925352 · 1993-01-12

Decision Date1993-01-12
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CLEAN CUFF BLOOD PRESSURE CUFF LINER is the device name listed in this FDA 510(k) record. The listed applicant is Steridyne Corp.. It received FDA 510(k) clearance on 1993-01-12 under 510(k) number K925352. 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 CLEAN CUFF BLOOD PRESSURE CUFF LINER?

CLEAN CUFF BLOOD PRESSURE CUFF LINER is a medical device that received FDA 510(k) clearance on 1993-01-12. The listed applicant is Steridyne Corp.. The 510(k) number is K925352.

When did CLEAN CUFF BLOOD PRESSURE CUFF LINER receive FDA 510(k) clearance?

CLEAN CUFF BLOOD PRESSURE CUFF LINER received FDA 510(k) clearance on 1993-01-12, under 510(k) number K925352.

Who is the listed applicant for CLEAN CUFF BLOOD PRESSURE CUFF LINER?

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

What is the FDA product code for CLEAN CUFF BLOOD PRESSURE CUFF LINER?

The FDA product code for CLEAN CUFF BLOOD PRESSURE CUFF LINER 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 Steridyne 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.

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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