Medsurg O.R. Procedure Tray

FDA 510(k) K914037 · Medsurg Industries, Inc.

Unknown

510(k) numberK914037

Submission

Device name
Medsurg O.R. Procedure Tray
Applicant
Medsurg Industries, Inc.
Herndon, VA, US
Received
September 10, 1991
Decision date
June 22, 1993
Decision
Unknown (SEKD)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
LRO – General Surgery Tray
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4370
Specialty
General, Plastic Surgery

This product code has been established in accordance with the may 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at www.Fda.Gov/cdrh/ode/convkit.Html. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance

Other 510(k)s with product code LRO

510(k)DeviceApplicantDecision
K213481Medline General Surgery TrayLRO · Traditional Medline Industries, Inc.05/24/2022SE
K212258Medline Cardiovascular Procedure KitLRO · Traditional Medline Industries, Inc.12/03/2021SE
K041080Surgical Drape Kit - D.I.R.R.A. SRLLRO · Traditional D.I.R.R.A. S.R.L.11/30/2004SE
K030721Quick-Tap Paracentesis Tray, Kit & NeedleLRO · Special Ballard Medical Products03/31/2003SE
K023276Amsino Tracheostomy Care TrayLRO · Traditional Amsino International, Inc.12/09/2002SE
K980137Worldwide Medical Technologies Bone Marrow Biopsy Procedure TrayLRO · Traditional Worldwide Medical Technologies, LLC01/30/1998SE
K971061Opportunity Inc. Bone Marrow Biopsy and Aspiration TrayLRO · Traditional Opportunity, Inc.06/11/1997SN
K971062Opportunity Inc. General Purpose TrayLRO · Traditional Opportunity, Inc.06/09/1997SN
K932221Neurological or Crani Trays (Packs)LRO · Traditional Associated Medical Products Co.03/19/1997SE
K970286Presbyterian Linen Services Surgical PacksLRO · Traditional Medline Industries, Inc.03/10/1997SE

More from Medline Industries, Inc.

510(k)DeviceDecision
K920780Medsurg Insertion TrayLFJ · Traditional 08/19/1994SEKD
K940175Medsurg Sterile O.R. TowelsKKX · Traditional 05/26/1994SE
K934731Medsurg Sterile Imaging ProductsFMP · Traditional 03/28/1994SE
K925558InfiltubeHIF · Traditional 03/04/1994SE
K934971Sterile Laparotomy SpongesGDY · Traditional 02/07/1994SE
K920421Medsurg Marshmallow TrayGAT · Traditional 12/13/1993SESK
K920838Medsurg Circumcision TrayHFK · Traditional 10/15/1993SE
K931932Dressing Change Tray-ModifiedMCY · Traditional 08/27/1993SEKD
K914036Medsurg Laparoscopy TrayLRO · Traditional 03/18/1992SE
K893938Continuous Epidural Anesthesia TrayCAZ · Traditional 08/07/1989SE

Questions and answers

When was Medsurg O.R. Procedure Tray cleared by the FDA?

Medsurg O.R. Procedure Tray (K914037) received a 510(k) decision of Unknown on June 22, 1993, 651 days after the submission was received.

What is the product code of K914037?

The FDA product code is LRO – General Surgery Tray, a Class II (moderate risk) device regulated under 21 CFR 878.4370.