FDA 510(k)

PILL PHONE

K-Number: K060298 · 2006-03-29

ApplicantVocel

Decision Date2006-03-29

Product CodeNXQ

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

PILL PHONE is the device name listed in this FDA 510(k) record. The listed applicant is Vocel. It received FDA 510(k) clearance on 2006-03-29 under 510(k) number K060298. 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 PILL PHONE?

PILL PHONE is a medical device that received FDA 510(k) clearance on 2006-03-29. The listed applicant is Vocel. The 510(k) number is K060298.

When did PILL PHONE receive FDA 510(k) clearance?

PILL PHONE received FDA 510(k) clearance on 2006-03-29, under 510(k) number K060298.

Who is the listed applicant for PILL PHONE?

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

What is the FDA product code for PILL PHONE?

The FDA product code for PILL PHONE 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)

K103009SENTICARE PILLSTATIONSenticare, Inc.

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.