MANAN INTRODUCER SHEALTH/NEEDLE
K-Number: K961216 · 1996-05-23
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Device Summary
Frequently Asked Questions
What is the MANAN INTRODUCER SHEALTH/NEEDLE?
MANAN INTRODUCER SHEALTH/NEEDLE is a medical device that received FDA 510(k) clearance on 1996-05-23. The listed applicant is Manan Medical Products, Inc.. The 510(k) number is K961216.
When did MANAN INTRODUCER SHEALTH/NEEDLE receive FDA 510(k) clearance?
MANAN INTRODUCER SHEALTH/NEEDLE received FDA 510(k) clearance on 1996-05-23, under 510(k) number K961216.
Who is the listed applicant for MANAN INTRODUCER SHEALTH/NEEDLE?
The FDA 510(k) record lists Manan Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MANAN INTRODUCER SHEALTH/NEEDLE?
The FDA product code for MANAN INTRODUCER SHEALTH/NEEDLE is FGE.
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 Manan 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: FGE)
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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