#ES-32 SUCTION CATHETER 32 FR.
K-Number: K970890 · 1997-05-23
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Device Summary
Frequently Asked Questions
What is the #ES-32 SUCTION CATHETER 32 FR.?
#ES-32 SUCTION CATHETER 32 FR. is a medical device that received FDA 510(k) clearance on 1997-05-23. The listed applicant is Tri-Med Specialties, Inc.. The 510(k) number is K970890.
When did #ES-32 SUCTION CATHETER 32 FR. receive FDA 510(k) clearance?
#ES-32 SUCTION CATHETER 32 FR. received FDA 510(k) clearance on 1997-05-23, under 510(k) number K970890.
Who is the listed applicant for #ES-32 SUCTION CATHETER 32 FR.?
The FDA 510(k) record lists Tri-Med Specialties, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for #ES-32 SUCTION CATHETER 32 FR.?
The FDA product code for #ES-32 SUCTION CATHETER 32 FR. is KNT.
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 Specialties, 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: KNT)
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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