Central Line Tray

FDA 510(k) K936117 · Cush Medical Products

Substantially Equivalent

510(k) numberK936117

Submission

Device name
Central Line Tray
Applicant
Cush Medical Products
Piney Flats, TN, US
Received
December 23, 1993
Decision date
March 1, 1994
Decision
Substantially Equivalent (SESE)
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
K943424Cush Island DressingMGP · Traditional 10/03/1994SN
K940518C-Section TrayMLS · Traditional 08/18/1994SEKD
K941349Dental TrayEIA · Traditional 07/26/1994SN
K941645Biopsy TrayFRG · Traditional 07/14/1994SEKD
K940239Eye TrayLRP · Traditional 06/28/1994SEKD
K935684IV Start KitLRS · Traditional 06/10/1994SEKD
K941455Sterile Gauze Product LineEFQ · Traditional 05/20/1994SESK
K941522Sterile X-Ray Detectable Gauze SpongesGDY · Traditional 05/12/1994SE
K941344Lap Sponge Product LineGDY · Traditional 05/12/1994SE
K935697Circumcision TrayHFX · Traditional 05/02/1994SEKD

Questions and answers

When was Central Line Tray cleared by the FDA?

Central Line Tray (K936117) received a 510(k) decision of Substantially Equivalent on March 1, 1994, 68 days after the submission was received.

What is the product code of K936117?

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