Irrigation/Suction Probe

FDA 510(k) K923667 · Surgical Instrument, Inc.

Substantially Equivalent

510(k) numberK923667

Submission

Device name
Irrigation/Suction Probe
Applicant
Surgical Instrument, Inc.
Placentia, CA, US
Received
July 22, 1992
Decision date
April 23, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

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/Suction Probe cleared by the FDA?

Irrigation/Suction Probe (K923667) received a 510(k) decision of Substantially Equivalent on April 23, 1993, 275 days after the submission was received.

What is the product code of K923667?

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