NEEDLELESS TRANSFER DEVICE
K-Number: K001831 · 2000-07-11
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Device Summary
Frequently Asked Questions
What is the NEEDLELESS TRANSFER DEVICE?
NEEDLELESS TRANSFER DEVICE is a medical device that received FDA 510(k) clearance on 2000-07-11. The listed applicant is Medimop Medical Projects, Ltd.. The 510(k) number is K001831.
When did NEEDLELESS TRANSFER DEVICE receive FDA 510(k) clearance?
NEEDLELESS TRANSFER DEVICE received FDA 510(k) clearance on 2000-07-11, under 510(k) number K001831.
Who is the listed applicant for NEEDLELESS TRANSFER DEVICE?
The FDA 510(k) record lists Medimop Medical Projects, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NEEDLELESS TRANSFER DEVICE?
The FDA product code for NEEDLELESS TRANSFER DEVICE is LHI.
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 Medimop Medical Projects, Ltd. 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: LHI)
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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