Intelijet Suction Supply

FDA 510(k) K922176 · Smith & Nephew Dyonics, Inc.

Substantially Equivalent

510(k) numberK922176

Submission

Device name
Intelijet Suction Supply
Applicant
Smith & Nephew Dyonics, Inc.
Andover, MA, US
Received
May 8, 1992
Decision date
November 18, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
BTA – Pump, Portable, Aspiration (Manual Or Powered)
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4780
Specialty
General, Plastic Surgery

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K953387Ectra Ligament Release SystemHRX · Traditional 08/09/1995SE
K945182Dyonics Fixation ScrewsHWC · Traditional 01/24/1995SN
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K934299Dyonics Disposable Arthroscopic Surgery Blades ModificationHRX · Traditional 02/14/1994SE
K920267Dyonics Arthroscopic KitLRO · Traditional 03/23/1993SEKD
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Questions and answers

When was Intelijet Suction Supply cleared by the FDA?

Intelijet Suction Supply (K922176) received a 510(k) decision of Substantially Equivalent on November 18, 1992, 194 days after the submission was received.

What is the product code of K922176?

The FDA product code is BTA – Pump, Portable, Aspiration (Manual Or Powered), a Class II (moderate risk) device regulated under 21 CFR 878.4780.