Single Use Instrument Tray

FDA 510(k) K951149 · Medcare Custom Packaging, Inc.

Unknown

510(k) numberK951149

Submission

Device name
Single Use Instrument Tray
Applicant
Medcare Custom Packaging, Inc.
East Swanzey, NH, US
Received
March 13, 1995
Decision date
April 6, 1995
Decision
Unknown (SESK)
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
K954869Medcare Yankauer Suction DeviceGCX · Traditional 01/19/1996SE
K954442Sterile Isotonic Saline & Sterile WaterJOL · Traditional 12/21/1995SE
K952759Towel PackKKX · Traditional 09/29/1995SE
K950390Urethral Catheterization TrayFCM · Traditional 05/30/1995SE
K943661Sterile Physiological Saline/Sterile WaterJOL · Traditional 04/10/1995SE
K934732Pelvic Exam TrayHHT · Traditional 12/30/1994SE
K942000Burn Dressing TrayFRG · Traditional 05/20/1994SESK
K936261Catheter Insertion TrayFMI · Traditional 03/10/1994SESK
K922179Catheter Insertion TrayFMI · Traditional 07/02/1993SEKD
K901856Custom Wound Management Kits and TraysLRO · Traditional 08/01/1990SESD

Questions and answers

When was Single Use Instrument Tray cleared by the FDA?

Single Use Instrument Tray (K951149) received a 510(k) decision of Unknown on April 6, 1995, 24 days after the submission was received.

What is the product code of K951149?

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