QUICK-TAP PARACENTESIS TRAY, KIT & NEEDLE
K-Number: K030721 · 2003-03-31
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Device Summary
Frequently Asked Questions
What is the QUICK-TAP PARACENTESIS TRAY, KIT & NEEDLE?
QUICK-TAP PARACENTESIS TRAY, KIT & NEEDLE is a medical device that received FDA 510(k) clearance on 2003-03-31. The listed applicant is Ballard Medical Products. The 510(k) number is K030721.
When did QUICK-TAP PARACENTESIS TRAY, KIT & NEEDLE receive FDA 510(k) clearance?
QUICK-TAP PARACENTESIS TRAY, KIT & NEEDLE received FDA 510(k) clearance on 2003-03-31, under 510(k) number K030721.
Who is the listed applicant for QUICK-TAP PARACENTESIS TRAY, KIT & NEEDLE?
The FDA 510(k) record lists Ballard Medical Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for QUICK-TAP PARACENTESIS TRAY, KIT & NEEDLE?
The FDA product code for QUICK-TAP PARACENTESIS TRAY, KIT & NEEDLE is LRO.
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 Ballard Medical Products 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: LRO)
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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