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FDA 510(k)

SURE FLOW TUBING

K-Number: K800664 · 1980-04-02

Decision Date1980-04-02
Product CodeBYX
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SURE FLOW TUBING is the device name listed in this FDA 510(k) record. The listed applicant is B & F Medical Products, Inc.. It received FDA 510(k) clearance on 1980-04-02 under 510(k) number K800664. The device is classified under product code BYX. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURE FLOW TUBING?

SURE FLOW TUBING is a medical device that received FDA 510(k) clearance on 1980-04-02. The listed applicant is B & F Medical Products, Inc.. The 510(k) number is K800664.

When did SURE FLOW TUBING receive FDA 510(k) clearance?

SURE FLOW TUBING received FDA 510(k) clearance on 1980-04-02, under 510(k) number K800664.

Who is the listed applicant for SURE FLOW TUBING?

The FDA 510(k) record lists B & F Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURE FLOW TUBING?

The FDA product code for SURE FLOW TUBING is BYX.

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 B & F Medical Products, 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 18 devices →

Related Devices (Code: BYX)

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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