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FDA 510(k)

ALL PURPOSE CUFF, MODEL 222APC

K-Number: K051904 · 2005-09-09

ApplicantSuntech Medical, Inc.
Decision Date2005-09-09
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ALL PURPOSE CUFF, MODEL 222APC is the device name listed in this FDA 510(k) record. The listed applicant is Suntech Medical, Inc.. It received FDA 510(k) clearance on 2005-09-09 under 510(k) number K051904. 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 ALL PURPOSE CUFF, MODEL 222APC?

ALL PURPOSE CUFF, MODEL 222APC is a medical device that received FDA 510(k) clearance on 2005-09-09. The listed applicant is Suntech Medical, Inc.. The 510(k) number is K051904.

When did ALL PURPOSE CUFF, MODEL 222APC receive FDA 510(k) clearance?

ALL PURPOSE CUFF, MODEL 222APC received FDA 510(k) clearance on 2005-09-09, under 510(k) number K051904.

Who is the listed applicant for ALL PURPOSE CUFF, MODEL 222APC?

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

What is the FDA product code for ALL PURPOSE CUFF, MODEL 222APC?

The FDA product code for ALL PURPOSE CUFF, MODEL 222APC is DXQ.

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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.

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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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