PARACENTESIS TRAYS
K-Number: K961863 · 1996-05-28
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Device Summary
Frequently Asked Questions
What is the PARACENTESIS TRAYS?
PARACENTESIS TRAYS is a medical device that received FDA 510(k) clearance on 1996-05-28. The listed applicant is Tri-Med, Inc.. The 510(k) number is K961863.
When did PARACENTESIS TRAYS receive FDA 510(k) clearance?
PARACENTESIS TRAYS received FDA 510(k) clearance on 1996-05-28, under 510(k) number K961863.
Who is the listed applicant for PARACENTESIS TRAYS?
The FDA 510(k) record lists Tri-Med, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PARACENTESIS TRAYS?
The FDA product code for PARACENTESIS TRAYS 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 Tri-Med, 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: 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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