Disposable Blood Line Connectors

FDA 510(k) K821495 · Bentley Laboratories, Inc.

Substantially Equivalent

510(k) numberK821495

Submission

Device name
Disposable Blood Line Connectors
Applicant
Bentley Laboratories, Inc.
Mchenry, IL, US
Received
May 19, 1982
Decision date
May 27, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KOC – Accessories, Blood Circuit, Hemodialysis
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5820
Specialty
Gastroenterology, Urology
Life-sustaining
Yes

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Questions and answers

When was Disposable Blood Line Connectors cleared by the FDA?

Disposable Blood Line Connectors (K821495) received a 510(k) decision of Substantially Equivalent on May 27, 1982, 8 days after the submission was received.

What is the product code of K821495?

The FDA product code is KOC – Accessories, Blood Circuit, Hemodialysis, a Class II (moderate risk) device regulated under 21 CFR 876.5820.