Primary Surgical Dressing Tray

FDA 510(k) K922041 · Transidyne General Corp.

Unknown

510(k) numberK922041

Submission

Device name
Primary Surgical Dressing Tray
Applicant
Transidyne General Corp.
Spartanburg, SC, US
Received
May 1, 1992
Decision date
November 6, 1992
Decision
Unknown (SEKD)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
FMF – Syringe, Piston
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5860
Specialty
General Hospital

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More from Instylla, Inc.

510(k)DeviceDecision
K961217Bodily Fluid Disposal KitFXX · Traditional 07/25/1996SE
K955658Laceration TrayFRG · Traditional 01/25/1996SE
K950773Prophylaxis PackEGS · Traditional 03/31/1995SESK
K950743Oral Procedure PackEGS · Traditional 03/31/1995SESK
K950449Surgical BurGFF · Traditional 03/01/1995SE
K950403Surgical Saw BladesGFA · Traditional 02/21/1995SE
K924811I.V. Start KitLRS · Traditional 06/17/1993SEKD
K924243Tracheostomy Care KitJOH · Traditional 06/16/1993SEKD
K922339Suture Removal KitMCZ · Traditional 12/11/1992SESK
K897133Model 1050 - Umbilical Cord Blood Sampling KitCBT · Traditional 03/30/1990SE

Questions and answers

When was Primary Surgical Dressing Tray cleared by the FDA?

Primary Surgical Dressing Tray (K922041) received a 510(k) decision of Unknown on November 6, 1992, 189 days after the submission was received.

What is the product code of K922041?

The FDA product code is FMF – Syringe, Piston, a Class II (moderate risk) device regulated under 21 CFR 880.5860.