MARTECH ENDOSCOPIC INJECTION NEEDLE
K-Number: K960519 · 1996-05-01
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Device Summary
Frequently Asked Questions
What is the MARTECH ENDOSCOPIC INJECTION NEEDLE?
MARTECH ENDOSCOPIC INJECTION NEEDLE is a medical device that received FDA 510(k) clearance on 1996-05-01. The listed applicant is Martech Medical Products, Inc.. The 510(k) number is K960519.
When did MARTECH ENDOSCOPIC INJECTION NEEDLE receive FDA 510(k) clearance?
MARTECH ENDOSCOPIC INJECTION NEEDLE received FDA 510(k) clearance on 1996-05-01, under 510(k) number K960519.
Who is the listed applicant for MARTECH ENDOSCOPIC INJECTION NEEDLE?
The FDA 510(k) record lists Martech Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MARTECH ENDOSCOPIC INJECTION NEEDLE?
The FDA product code for MARTECH ENDOSCOPIC INJECTION NEEDLE is FBK.
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 Martech Medical 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: FBK)
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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