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FDA 510(k)

DANA EMULATING INDICATOR

K-Number: K100891 · 2011-01-13

ApplicantDana Products, Inc.
Decision Date2011-01-13
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DANA EMULATING INDICATOR is the device name listed in this FDA 510(k) record. The listed applicant is Dana Products, Inc.. It received FDA 510(k) clearance on 2011-01-13 under 510(k) number K100891. The device is classified under product code JOJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DANA EMULATING INDICATOR?

DANA EMULATING INDICATOR is a medical device that received FDA 510(k) clearance on 2011-01-13. The listed applicant is Dana Products, Inc.. The 510(k) number is K100891.

When did DANA EMULATING INDICATOR receive FDA 510(k) clearance?

DANA EMULATING INDICATOR received FDA 510(k) clearance on 2011-01-13, under 510(k) number K100891.

Who is the listed applicant for DANA EMULATING INDICATOR?

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

What is the FDA product code for DANA EMULATING INDICATOR?

The FDA product code for DANA EMULATING INDICATOR is JOJ.

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Other records listing Dana Products, Inc. as applicant

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Related Devices (Code: JOJ)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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