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FDA 510(k)

REUSABLE TEST PACK FOR DANA EMULATING INDICATORS

K-Number: K110253 · 2011-04-29

ApplicantDana Products, Inc.
Decision Date2011-04-29
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

REUSABLE TEST PACK FOR DANA EMULATING INDICATORS 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 2011-04-29 under 510(k) number K110253. 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 REUSABLE TEST PACK FOR DANA EMULATING INDICATORS?

REUSABLE TEST PACK FOR DANA EMULATING INDICATORS is a medical device that received FDA 510(k) clearance on 2011-04-29. The listed applicant is Dana Products, Inc.. The 510(k) number is K110253.

When did REUSABLE TEST PACK FOR DANA EMULATING INDICATORS receive FDA 510(k) clearance?

REUSABLE TEST PACK FOR DANA EMULATING INDICATORS received FDA 510(k) clearance on 2011-04-29, under 510(k) number K110253.

Who is the listed applicant for REUSABLE TEST PACK FOR DANA EMULATING INDICATORS?

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 REUSABLE TEST PACK FOR DANA EMULATING INDICATORS?

The FDA product code for REUSABLE TEST PACK FOR DANA EMULATING INDICATORS is JOJ.

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Other records listing Dana Products, Inc. as applicant

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.

K130135DANA REUSABLE BI TEST PACKK120592DANA REUSABLE BOWIE TEST PACK FOR DANA BOWIE DICK INDICATORSK103321DANA REUSABLE TESTPACK FOR STEAM STERILIZATION FOR 10 MINUTE EXTENDED CYCLESK100891DANA EMULATING INDICATORK102761DANA REUSABLE TEST PACK FOR STEAM STERILIZATIONK092944DANA REUSABLE TEST PACK FOR STEAM STERILIZATION

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Related Devices (Code: JOJ)

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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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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