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FDA 510(k)

TUBING CONNECTORS

K-Number: K860291 · 1986-03-31

ApplicantBiomedical Exports, Inc.
Decision Date1986-03-31
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TUBING CONNECTORS is the device name listed in this FDA 510(k) record. The listed applicant is Biomedical Exports, Inc.. It received FDA 510(k) clearance on 1986-03-31 under 510(k) number K860291. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUBING CONNECTORS?

TUBING CONNECTORS is a medical device that received FDA 510(k) clearance on 1986-03-31. The listed applicant is Biomedical Exports, Inc.. The 510(k) number is K860291.

When did TUBING CONNECTORS receive FDA 510(k) clearance?

TUBING CONNECTORS received FDA 510(k) clearance on 1986-03-31, under 510(k) number K860291.

Who is the listed applicant for TUBING CONNECTORS?

The FDA 510(k) record lists Biomedical Exports, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TUBING CONNECTORS?

The FDA product code for TUBING CONNECTORS is DTL.

Related Clinical Trials

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Other records listing Biomedical Exports, 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.

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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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