Blood Containment Pack

FDA 510(k) K872448 · Professional Medical Services

Substantially Equivalent

510(k) numberK872448

Submission

Device name
Blood Containment Pack
Applicant
Professional Medical Services
North Salt Lake, UT, US
Received
June 23, 1987
Decision date
November 17, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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
K913094Disposable Slide Valve ManifoldDQO · Traditional 01/27/1992SE
K910378Pressure Monitoring Extension LineDQO · Traditional 04/22/1991SE
K904508Condor Analog Inflation SyringeMAV · Traditional 04/02/1991SE
K904954Condor Digital Inflation SyringeMAV · Traditional 01/16/1991SE
K902606Radiopaque RulerKPR · Traditional 09/27/1990SE
K884577Procedure Ready TraysFOZ · Traditional 08/01/1989SESD
K890471PMS Angio DrapeKKX · Traditional 02/27/1989SE
K884497Control SyringeFMF · Traditional 12/12/1988SE
K8645553 Ring AttachmentFMF · Traditional 12/01/1986SE
K854941PMS Percutaneous Puncture NeedleDYB · Traditional 04/16/1986SE

Questions and answers

When was Blood Containment Pack cleared by the FDA?

Blood Containment Pack (K872448) received a 510(k) decision of Substantially Equivalent on November 17, 1987, 147 days after the submission was received.

What is the product code of K872448?

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