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FDA 510(k)

#ES-32 SUCTION CATHETER 32 FR.

K-Number: K970890 · 1997-05-23

Decision Date1997-05-23
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

#ES-32 SUCTION CATHETER 32 FR. is the device name listed in this FDA 510(k) record. The listed applicant is Tri-Med Specialties, Inc.. It received FDA 510(k) clearance on 1997-05-23 under 510(k) number K970890. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 14 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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