PTFE PORTABLE INTRODUCER
K-Number: K102540 · 2010-11-16
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Device Summary
Frequently Asked Questions
What is the PTFE PORTABLE INTRODUCER?
PTFE PORTABLE INTRODUCER is a medical device that received FDA 510(k) clearance on 2010-11-16. The listed applicant is Great Batch Medical. The 510(k) number is K102540.
When did PTFE PORTABLE INTRODUCER receive FDA 510(k) clearance?
PTFE PORTABLE INTRODUCER received FDA 510(k) clearance on 2010-11-16, under 510(k) number K102540.
Who is the listed applicant for PTFE PORTABLE INTRODUCER?
The FDA 510(k) record lists Great Batch Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PTFE PORTABLE INTRODUCER?
The FDA product code for PTFE PORTABLE INTRODUCER 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 Great Batch Medical 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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