ABCO SUCTION CATHETER & KITS W/GLOVE&CUP
K-Number: K800234 · 1980-02-26
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Device Summary
Frequently Asked Questions
What is the ABCO SUCTION CATHETER & KITS W/GLOVE&CUP?
ABCO SUCTION CATHETER & KITS W/GLOVE&CUP is a medical device that received FDA 510(k) clearance on 1980-02-26. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K800234.
When did ABCO SUCTION CATHETER & KITS W/GLOVE&CUP receive FDA 510(k) clearance?
ABCO SUCTION CATHETER & KITS W/GLOVE&CUP received FDA 510(k) clearance on 1980-02-26, under 510(k) number K800234.
Who is the listed applicant for ABCO SUCTION CATHETER & KITS W/GLOVE&CUP?
The FDA 510(k) record lists Abco Dealers, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ABCO SUCTION CATHETER & KITS W/GLOVE&CUP?
The FDA product code for ABCO SUCTION CATHETER & KITS W/GLOVE&CUP is JOL.
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 Abco Dealers, 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: JOL)
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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