Angio Med Disposable Pressure Connectors

FDA 510(k) K855078 · Angiomed U.S., Inc.

Substantially Equivalent

510(k) numberK855078

Submission

Device name
Angio Med Disposable Pressure Connectors
Applicant
Angiomed U.S., Inc.
Anaheim, CA, US
Received
December 19, 1985
Decision date
February 19, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KGZ – Accessories, Catheter
Device class
Class I (low risk)
Regulation
21 CFR 878.4200
Specialty
General, Plastic Surgery

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Questions and answers

When was Angio Med Disposable Pressure Connectors cleared by the FDA?

Angio Med Disposable Pressure Connectors (K855078) received a 510(k) decision of Substantially Equivalent on February 19, 1986, 62 days after the submission was received.

What is the product code of K855078?

The FDA product code is KGZ – Accessories, Catheter, a Class I (low risk) device regulated under 21 CFR 878.4200.