DANA REUSABLE BOWIE TEST PACK FOR DANA BOWIE DICK INDICATORS
K-Number: K120592 · 2013-02-27
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Device Summary
Frequently Asked Questions
What is the DANA REUSABLE BOWIE TEST PACK FOR DANA BOWIE DICK INDICATORS?
DANA REUSABLE BOWIE TEST PACK FOR DANA BOWIE DICK INDICATORS is a medical device that received FDA 510(k) clearance on 2013-02-27. The listed applicant is Dana Products, Inc.. The 510(k) number is K120592.
When did DANA REUSABLE BOWIE TEST PACK FOR DANA BOWIE DICK INDICATORS receive FDA 510(k) clearance?
DANA REUSABLE BOWIE TEST PACK FOR DANA BOWIE DICK INDICATORS received FDA 510(k) clearance on 2013-02-27, under 510(k) number K120592.
Who is the listed applicant for DANA REUSABLE BOWIE TEST PACK FOR DANA BOWIE DICK 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 DANA REUSABLE BOWIE TEST PACK FOR DANA BOWIE DICK INDICATORS?
The FDA product code for DANA REUSABLE BOWIE TEST PACK FOR DANA BOWIE DICK INDICATORS is JOJ.
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.
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.
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.
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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