Hyperalimentation Dressing Tray

FDA 510(k) K792369 · Pharmaseal Div., Baxter Healthcare Corp.

Substantially Equivalent

510(k) numberK792369

Submission

Device name
Hyperalimentation Dressing Tray
Applicant
Pharmaseal Div., Baxter Healthcare Corp.
Mchenry, IL, US
Received
September 24, 1979
Decision date
December 10, 1979
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FRG – Wrap, Sterilization
Device class
Class II (moderate risk)
Regulation
21 CFR 880.6850
Specialty
General Hospital

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K252823Dukal Crepe Paper Sterilization WrapFRG · Traditional Dukal, LLC05/28/2026SE
K253454HALYARD* ONE-STEP* Sterilization Wrap; HALYARD* QUICK CHECK* Sterilization Wrap…FRG · Traditional O&M Halyard, Inc.05/18/2026SE
K251347Sterilization Pouch/RollFRG · Traditional Sterivic Medical Co., Ltd.01/28/2026SE
K251177Self-Seal Sterilization Pouch and RollFRG · Traditional Guangdong Maidi Medical Co., Ltd.12/12/2025SE
K250306Chex-All Sterilization Pouches and TubesFRG · Abbreviated Propper Manufacturing Co., Inc.10/31/2025SE
K243179Sterilization Pouch and RollFRG · Traditional Yichang Xinxin Paper Products Co., Ltd.06/26/2025SE
K250321GCI Sterilization WrappersFRG · Traditional George Courey, Inc.06/06/2025SE
K243721Self Sealing Sterilization PouchesFRG · Traditional Wellmed Dental Medical Supply Co., Ltd.04/25/2025SE
K250011Turbett Surgical Instrument Pod (TS1500); Turbett Surgical Instrument Pod (TS1200)…FRG · Traditional Turbett Surgical04/04/2025SE

More from Turbett Surgical

510(k)DeviceDecision
K792141Continuous Flush DeviceKRA · Traditional 12/05/1979SE
K792019Phadecode Xa Inhibitor AssayJBQ · Traditional 11/05/1979SE
K791773Ventilator Tube with FilterCAH · Traditional 10/22/1979SE
K791156Amipaque Myelogram TrayFMI · Traditional 07/30/1979SE
K790896Two-Way Anesthesia FilterCAH · Traditional 06/05/1979SE
K790409Low Dead Space Insulin SyringeFMF · Traditional 04/24/1979SE
K782069Tray, Auxillary BlockCAZ · Traditional 01/04/1979SE
K781797Prep Tray, Preoperative SkinOJU · Traditional 11/08/1978SE
K781680Monitoring, Pressure KitDRS · Traditional 10/06/1978SE
K780887Improved Disposable Hypodermic NeedleGAA · Traditional 06/22/1978SE

Questions and answers

When was Hyperalimentation Dressing Tray cleared by the FDA?

Hyperalimentation Dressing Tray (K792369) received a 510(k) decision of Substantially Equivalent on December 10, 1979, 77 days after the submission was received.

What is the product code of K792369?

The FDA product code is FRG – Wrap, Sterilization, a Class II (moderate risk) device regulated under 21 CFR 880.6850.