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FDA 510(k)

BLOOD VESSEL CONNECTOR

K-Number: K871408 · 1987-04-27

ApplicantQuali-Med, Inc.
Decision Date1987-04-27
Product Code
DecisionSubstantially Equivalent

Device Summary

BLOOD VESSEL CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Quali-Med, Inc.. It received FDA 510(k) clearance on 1987-04-27 under 510(k) number K871408. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOD VESSEL CONNECTOR?

BLOOD VESSEL CONNECTOR is a medical device that received FDA 510(k) clearance on 1987-04-27. The listed applicant is Quali-Med, Inc.. The 510(k) number is K871408.

When did BLOOD VESSEL CONNECTOR receive FDA 510(k) clearance?

BLOOD VESSEL CONNECTOR received FDA 510(k) clearance on 1987-04-27, under 510(k) number K871408.

Who is the listed applicant for BLOOD VESSEL CONNECTOR?

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

Related Clinical Trials

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Other records listing Quali-Med, 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.

K862972DISPOSABLE MIRRORK862472QUARTZ RODS TITANIUM RODSK862241STANDARD BASIN KIT CUSTOM BASIN KITK862242PAP SMEAR KITK862172QUALI-MED'S OPERATING ROOM DRAPESK861198CUSTOM PROCEDURE KIT (VARIOUS SUB-TITLES)

View all 7 devices →

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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