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FDA 510(k)

MULTI-PURPOSE HEALTH DEVICE

K-Number: K093322 · 2010-08-05

Decision Date2010-08-05
Product CodeBWK
DecisionSubstantially Equivalent

Device Summary

MULTI-PURPOSE HEALTH DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Upc Medical Supplies, Inc. Dba United Pacific Co.. It received FDA 510(k) clearance on 2010-08-05 under 510(k) number K093322. The device is classified under product code BWK. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTI-PURPOSE HEALTH DEVICE?

MULTI-PURPOSE HEALTH DEVICE is a medical device that received FDA 510(k) clearance on 2010-08-05. The listed applicant is Upc Medical Supplies, Inc. Dba United Pacific Co.. The 510(k) number is K093322.

When did MULTI-PURPOSE HEALTH DEVICE receive FDA 510(k) clearance?

MULTI-PURPOSE HEALTH DEVICE received FDA 510(k) clearance on 2010-08-05, under 510(k) number K093322.

Who is the listed applicant for MULTI-PURPOSE HEALTH DEVICE?

The FDA 510(k) record lists Upc Medical Supplies, Inc. Dba United Pacific Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTI-PURPOSE HEALTH DEVICE?

The FDA product code for MULTI-PURPOSE HEALTH DEVICE is BWK.

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: BWK)

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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