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FDA 510(k)

SENTICARE PILLSTATION

K-Number: K103009 · 2011-01-28

ApplicantSenticare, Inc.
Decision Date2011-01-28
Product CodeNXQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SENTICARE PILLSTATION is the device name listed in this FDA 510(k) record. The listed applicant is Senticare, Inc.. It received FDA 510(k) clearance on 2011-01-28 under 510(k) number K103009. The device is classified under product code NXQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SENTICARE PILLSTATION?

SENTICARE PILLSTATION is a medical device that received FDA 510(k) clearance on 2011-01-28. The listed applicant is Senticare, Inc.. The 510(k) number is K103009.

When did SENTICARE PILLSTATION receive FDA 510(k) clearance?

SENTICARE PILLSTATION received FDA 510(k) clearance on 2011-01-28, under 510(k) number K103009.

Who is the listed applicant for SENTICARE PILLSTATION?

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

What is the FDA product code for SENTICARE PILLSTATION?

The FDA product code for SENTICARE PILLSTATION is NXQ.

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.

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Related Devices (Code: NXQ)

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.

K060298PILL PHONEVocel

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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