MICROSLIDER TEARAWAY INTRODUCER SET
K-Number: K123430 · 2013-04-12
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Device Summary
Frequently Asked Questions
What is the MICROSLIDER TEARAWAY INTRODUCER SET?
MICROSLIDER TEARAWAY INTRODUCER SET is a medical device that received FDA 510(k) clearance on 2013-04-12. The listed applicant is Galt Medical Corp.. The 510(k) number is K123430.
When did MICROSLIDER TEARAWAY INTRODUCER SET receive FDA 510(k) clearance?
MICROSLIDER TEARAWAY INTRODUCER SET received FDA 510(k) clearance on 2013-04-12, under 510(k) number K123430.
Who is the listed applicant for MICROSLIDER TEARAWAY INTRODUCER SET?
The FDA 510(k) record lists Galt Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICROSLIDER TEARAWAY INTRODUCER SET?
The FDA product code for MICROSLIDER TEARAWAY INTRODUCER SET is DYB.
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 Galt Medical Corp. 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: DYB)
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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