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FDA 510(k)

VERESURE BELL

K-Number: K061387 · 2006-07-21

ApplicantVeresure, Inc.
Decision Date2006-07-21
Product CodeHIF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

VERESURE BELL is the device name listed in this FDA 510(k) record. The listed applicant is Veresure, Inc.. It received FDA 510(k) clearance on 2006-07-21 under 510(k) number K061387. The device is classified under product code HIF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERESURE BELL?

VERESURE BELL is a medical device that received FDA 510(k) clearance on 2006-07-21. The listed applicant is Veresure, Inc.. The 510(k) number is K061387.

When did VERESURE BELL receive FDA 510(k) clearance?

VERESURE BELL received FDA 510(k) clearance on 2006-07-21, under 510(k) number K061387.

Who is the listed applicant for VERESURE BELL?

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

What is the FDA product code for VERESURE BELL?

The FDA product code for VERESURE BELL is HIF.

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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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