#014160-TAB TUBING ROTATOR ADAPTOR— 510(k) K870325

Name: FDA 510(k) clearance K870325
Creator: U.S. Food and Drug Administration
Published: 1987-04-27

Substantially Equivalent

Clinical Connections, Inc.

FDA 510(k) clearance K870325 for #014160-TAB TUBING ROTATOR ADAPTOR, Substantially Equivalent on 1987-04-27. Applicant: Clinical Connections, Inc.. Device class: 2.

Clearance details

Applicant: Clinical Connections, Inc.
Product code: Code DTL
Device class: Class 2
Regulation: 21 CFR 870.4290
Advisory panel: Cardiovascular
Date received: 1987-01-28
Decision date: 1987-04-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Orrville, OH, US

Download summary PDF View on FDA.gov ↗

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K884435 — RESUBMITTED 1,3 & 4 WAY STOPCOCKS, VARIOUS PARTS1988-11-08
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K870477 — DEVICE CONNECTORS #000299-000 3/8 X 3/8 X 3/8 Y1987-04-03
K870912 — T-CONNECTORS 014500/014501/014502/014503-1201987-03-17
K870913 — INJECTION SITE #014456-1201987-03-17

Adverse events under product code DTL

product code DTL

Malfunction: 770
Total: 770

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.