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FDA 510(k)

ABCO CONNECTING TUBES PRECUT LENGTHS

K-Number: K800235 · 1980-02-26

ApplicantAbco Dealers, Inc.
Decision Date1980-02-26
Product CodeBYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ABCO CONNECTING TUBES PRECUT LENGTHS is the device name listed in this FDA 510(k) record. The listed applicant is Abco Dealers, Inc.. It received FDA 510(k) clearance on 1980-02-26 under 510(k) number K800235. The device is classified under product code BYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABCO CONNECTING TUBES PRECUT LENGTHS?

ABCO CONNECTING TUBES PRECUT LENGTHS 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 K800235.

When did ABCO CONNECTING TUBES PRECUT LENGTHS receive FDA 510(k) clearance?

ABCO CONNECTING TUBES PRECUT LENGTHS received FDA 510(k) clearance on 1980-02-26, under 510(k) number K800235.

Who is the listed applicant for ABCO CONNECTING TUBES PRECUT LENGTHS?

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 CONNECTING TUBES PRECUT LENGTHS?

The FDA product code for ABCO CONNECTING TUBES PRECUT LENGTHS is BYY.

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Other records listing Abco Dealers, Inc. as applicant

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Related Devices (Code: BYY)

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.

K960616VITAFLOW SUCTION/ASPIRATION TUBING SETVital Concepts, Inc.K960218CONNECTING TUBINGCustom Pack ReliabilityK955151MAXI-FLOW SUCTION TUBE/TOP GUN SUCTION IRRIGATORBio-Medical Devices, Inc.K955149MAXI-FLOW SUCTION HANDLE/THE REEL THING TUBING REELBio-Medical Devices, Inc.K955150MAXI-FLOWBio-Medical Devices, Inc.K922989WILTEK IRRIGAITON/ASPIRATION TUBE SETWiltek Medical, Inc.

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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