General Purpose Instrument Tray, Sterile, Disposab

FDA 510(k) K920516 · Trinity Laboratories, Inc.

Unknown

510(k) numberK920516

Submission

Device name
General Purpose Instrument Tray, Sterile, Disposab
Applicant
Trinity Laboratories, Inc.
Salisbury, MD, US
Received
February 4, 1992
Decision date
April 16, 1992
Decision
Unknown (SEKD)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
KDD – Kit, Surgical Instrument, Disposable
Device class
Class I (low risk)
Regulation
21 CFR 878.4800
Specialty
General, Plastic Surgery

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K932219Suture Set or Laceration Trays (Packs)KDD · Traditional Associated Medical Products Co.07/09/1993SESK
K923176Surgical Instrument Kit, DisposableKDD · Traditional Ulti-Med Intl., Inc.06/17/1993SE
K925905Kit, Surgical Instrument, DisposableKDD · Traditional Kay Medical Concepts06/16/1993SESK
K924958Biopsy/Myelo/Arthro/Amniocent/Basic Skin Prep TrayKDD · Traditional Medical Insights, Inc.06/07/1993SEKD
K925215Sterile Surgical Instrument TraysKDD · Traditional American Healthcare Supply Co., Inc.06/01/1993SEKD

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K972160Crp-Lex System: C-Reactive Protein Antigen Detection in Serum: Slide Agglutnation Latex…DCK · Traditional 08/01/1997SE
K970722Eye TrayKKX · Traditional 03/31/1997SE
K965201O.R. Scrub Prep Tray, Sterile, DisposableLRO · Traditional 02/14/1997SEKD
K964921Basic Biopsy Tray. Disposable, SterileLRO · Traditional 01/22/1997SE
K953929Mid-Stream Collection Set-SterileLIO · Traditional 11/16/1995SE
K952058Sterile V.A.D. (Vascular Access Devices) Access Kit, DisposableFOZ · Traditional 09/21/1995SE
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Questions and answers

When was General Purpose Instrument Tray, Sterile, Disposab cleared by the FDA?

General Purpose Instrument Tray, Sterile, Disposab (K920516) received a 510(k) decision of Unknown on April 16, 1992, 72 days after the submission was received.

What is the product code of K920516?

The FDA product code is KDD – Kit, Surgical Instrument, Disposable, a Class I (low risk) device regulated under 21 CFR 878.4800.