Endo Optiks Value Pack

FDA 510(k) K923600 · Endo Optics, Inc.

Unknown

510(k) numberK923600

Submission

Device name
Endo Optiks Value Pack
Applicant
Endo Optics, Inc.
Marlboro, NJ, US
Received
July 20, 1992
Decision date
March 23, 1993
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

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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
K924090The Endo Optiks MicroprobeHQB · Traditional 02/01/1993SE

Questions and answers

When was Endo Optiks Value Pack cleared by the FDA?

Endo Optiks Value Pack (K923600) received a 510(k) decision of Unknown on March 23, 1993, 246 days after the submission was received.

What is the product code of K923600?

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