GRIPPER PLUS NEEDLE
K-Number: K021999 · 2002-08-13
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Device Summary
Frequently Asked Questions
What is the GRIPPER PLUS NEEDLE?
GRIPPER PLUS NEEDLE is a medical device that received FDA 510(k) clearance on 2002-08-13. The listed applicant is Deltec, Inc.. The 510(k) number is K021999.
When did GRIPPER PLUS NEEDLE receive FDA 510(k) clearance?
GRIPPER PLUS NEEDLE received FDA 510(k) clearance on 2002-08-13, under 510(k) number K021999.
Who is the listed applicant for GRIPPER PLUS NEEDLE?
The FDA 510(k) record lists Deltec, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GRIPPER PLUS NEEDLE?
The FDA product code for GRIPPER PLUS NEEDLE is FPA.
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 Deltec, 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: FPA)
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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