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FDA 510(k)

HOCA EZ-CARE BP108, TENDER-CARE BP109

K-Number: K052671 · 2006-02-03

Decision Date2006-02-03
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HOCA EZ-CARE BP108, TENDER-CARE BP109 is the device name listed in this FDA 510(k) record. The listed applicant is Hoca Medical Microsystem, Inc.. It received FDA 510(k) clearance on 2006-02-03 under 510(k) number K052671. 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 HOCA EZ-CARE BP108, TENDER-CARE BP109?

HOCA EZ-CARE BP108, TENDER-CARE BP109 is a medical device that received FDA 510(k) clearance on 2006-02-03. The listed applicant is Hoca Medical Microsystem, Inc.. The 510(k) number is K052671.

When did HOCA EZ-CARE BP108, TENDER-CARE BP109 receive FDA 510(k) clearance?

HOCA EZ-CARE BP108, TENDER-CARE BP109 received FDA 510(k) clearance on 2006-02-03, under 510(k) number K052671.

Who is the listed applicant for HOCA EZ-CARE BP108, TENDER-CARE BP109?

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

What is the FDA product code for HOCA EZ-CARE BP108, TENDER-CARE BP109?

The FDA product code for HOCA EZ-CARE BP108, TENDER-CARE BP109 is DXN.

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: 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.

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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