ABDOMINAL PARACENTESIS TRAY
K-Number: K842009 · 1984-10-23
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Device Summary
Frequently Asked Questions
What is the ABDOMINAL PARACENTESIS TRAY?
ABDOMINAL PARACENTESIS TRAY is a medical device that received FDA 510(k) clearance on 1984-10-23. The listed applicant is Jayco Pharmaceuticals. The 510(k) number is K842009.
When did ABDOMINAL PARACENTESIS TRAY receive FDA 510(k) clearance?
ABDOMINAL PARACENTESIS TRAY received FDA 510(k) clearance on 1984-10-23, under 510(k) number K842009.
Who is the listed applicant for ABDOMINAL PARACENTESIS TRAY?
The FDA 510(k) record lists Jayco Pharmaceuticals as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ABDOMINAL PARACENTESIS TRAY?
The FDA product code for ABDOMINAL PARACENTESIS TRAY is FSM.
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 Jayco Pharmaceuticals 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: FSM)
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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