Irrigation Catheter

FDA 510(k) K780788 · Shiley, Inc.

Substantially Equivalent

510(k) numberK780788

Submission

Device name
Irrigation Catheter
Applicant
Shiley, Inc.
Mchenry, IL, US
Received
May 15, 1978
Decision date
June 22, 1978
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

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

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Questions and answers

When was Irrigation Catheter cleared by the FDA?

Irrigation Catheter (K780788) received a 510(k) decision of Substantially Equivalent on June 22, 1978, 38 days after the submission was received.

What is the product code of K780788?

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